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Assessment of the strength of the trunk and upper limb muscles in stroke subjects with portable dynamometry: a literature review

Avaliação da força muscular pós-AVE pela dinamometria portátil: uma revisão da literatura

Abstracts

Introduction

Clinical measurements of strength in stroke subjects are usually performed and portable dynamometers are one of the most employed instruments.

Objective

To verify the standardization procedures of the methods used to assess the strength of the trunk and upper limb muscles with portable dynamometers in stroke subjects, as well as to assess the psychometric properties which were already investigated.

Materials and methods

An extensive search was performed on the MEDLINE, SciELO, LILACS, and PEDro databases, by combining specific key words, followed by active manual searches by two independent researchers.

Results and discussion

Fifty-eight studies were included: three related to the trunk and 55 to the upper limb muscles, including handgrip and pinch strength assessments. The most investigated muscular groups were handgrip, elbow flexors/extensors, wrist extensors, and lateral pinch. Nine studies reported adequate reliability levels and the seated position was employed in the majority of the studies which assessed trunk, handgrip, and pinch strength, while the supine position was used for the other muscular groups. The number of trials most used was three, while the reported contractions and rest times were variable.

Final considerations

Most studies reported the positioning and/or the data collection protocols; however, there was no consensus on the standardization procedures. The only investigated psychometric property was reliability. Few studies evaluated the trunk muscles and other psychometric properties.

Dynamometer; Trunk; Upper limbs; Reliability; Validity


Introdução

A mensuração da força muscular em indivíduos acometidos pelo Acidente Vascular Encefálico (AVE) é comumente realizada na clínica, sendo os dinamômetros portáteis os instrumentos mais utilizados para tanto.

Objetivo

Verificar se há uma padronização dos métodos utilizados para avaliação da força muscular de tronco e membros superiores (MMSS) com o uso de dinamômetros portáteis em indivíduos pós-AVE, bem como verificar quais propriedades de medida já foram investigadas.

Materiais e métodos

As buscas foram realizadas nas bases de dados MEDLINE, SciELO, LILACS e PEDro com combinação de termos específicos, seguidas de busca manual ativa. A seleção dos estudos e a extração das informações foram realizadas por dois examinadores independentes.

Resultados e discussão

Foram incluídos 58 estudos (três de tronco e 55 de MMSS, incluindo preensão manual e pinça). Os grupos musculares mais avaliados foram preensão manual, flexores de cotovelo, extensores de punho, extensores de cotovelo e pinça lateral. Nove estudos reportaram confiabilidade adequada do método. A maioria dos estudos que avaliaram os músculos de tronco, de preensão manual e de pinça utilizou a postura sentada, enquanto o decúbito dorsal foi mais utilizado na avaliação dos demais músculos. O número de repetições mais utilizado foi três, já o tempo de contração e o período de repouso variaram entre os estudos.

Considerações finais

A maioria dos estudos relatou o posicionamento e/ou o protocolo de coleta, porém não houve uma padronização. A única propriedade de medida investigada foi a confiabilidade. Poucos estudos avaliaram os músculos de tronco e as outras propriedades de medida.

Dinamômetro; Tronco; Membros superiors; Confiabilidade; Validade


Introduction

Stroke is an important cause of disabilities. Every year, thousands of working-age adults become partially or totally disabled by this health condition (1Lopez A, Mathers C, Ezzati M, Jamison D, Murray C. Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data. Lancet. 2006;367(9524):1747-57.), which results in emotional distresses for the patients and their families and socio-economic impact on the health systems (2World Health Organization. Neurological disorders: public health challenges. Geneva: WHO Library Cateloguin-in-Publication Data; 2006.). Stroke subjects may demonstrate several impairments, being the motor ones the most common (3Ada L, Dorsch S, Canning CG. Strengthening interventions increase strength and improve activity after stroke: a systematic review. Aust J Physiother. 2006; 52(4):241-8.

Kamper D, Fischer H, Cruz E, Rymer W. Weakness is the primary contributor to finger impairment in chronic stroke. Arch Phys Med Rehabil. 2006;87(9):1262-9.
-5Bohannon RW. Muscle strength and muscle training after stroke. J Rehabil Med. 2007;39(1):14-20.) and those that affect the performance of daily life activities (6Abe I. Prevalência de acidente vascular cerebral em área de exclusão social na cidade de São Paulo, Brasil: utilizando questionário validado para sintomas [tese]. São Paulo: Universidade de São Paulo; 2010.).

Among the observed motor impairments, muscular weakness has shown significant associations with activity limitations (3Ada L, Dorsch S, Canning CG. Strengthening interventions increase strength and improve activity after stroke: a systematic review. Aust J Physiother. 2006; 52(4):241-8., 7Faria-Fortini I, Michaelsen S, Cassiano J, Teixeira-Salmela L. Upper extremity function in stroke subjects: relationships between the International Classification of Functioning, Disability, and Health Domains. J Hand Ther. 2011;24(3):257-65., 8Kwakkel G, Kollen B. Predicting improvement in the upper paretic limb after stroke: a longitudinal prospective study. Restor Neurol Neurosci. 2007; 25(5-6):453-60.) and social participation restriction (7Faria-Fortini I, Michaelsen S, Cassiano J, Teixeira-Salmela L. Upper extremity function in stroke subjects: relationships between the International Classification of Functioning, Disability, and Health Domains. J Hand Ther. 2011;24(3):257-65., 8Kwakkel G, Kollen B. Predicting improvement in the upper paretic limb after stroke: a longitudinal prospective study. Restor Neurol Neurosci. 2007; 25(5-6):453-60.). Specifically, weakness of the upper limb (UL) (9Boissy P, Bourbonnais D, Carlotti MM, Gravel D, Arsenault BA. Maximal grip force in chronic stroke subjects and its relationship to global upper extremity function. Clin Rehabil. 1999;13(4):354-62.

10 Mercier C, Bourbounais D. Relative shoulder flexor and handgrip strength is related to upper limb function after stroke. Clin Rehabil. 2004;18(2):215-21.

11 Nascimento L. Desempenho muscular isocinético do complexo do ombro de indivíduos com hemiparesia crônica [dissertação]. Belo Horizonte: Universidade Federal de Minas Gerais; 2011.

12 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72.
-1313 Harris JE, Eng JJ. Paretic upper-limb strength best explains arm activity in people with stroke. Phys Ther. 2007;87(1):88-97.) and trunk (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 1515 Karatas M, Çetin N, Bayramoglu M, Dilek A. Trunk muscle strength in relation to balance and functional disability in unihemispheric stroke patients. Am J Phys Med Rehabil. 2004;83(2):81-7.) muscles, which are involved in the performance of many basic, instrumental, work, and leisure activities, lead to important functional limitations. About 70% of the subjects with paresis of the UL muscles have some degree of functional limitation (1313 Harris JE, Eng JJ. Paretic upper-limb strength best explains arm activity in people with stroke. Phys Ther. 2007;87(1):88-97., 1616 Oullette MM, LeBrasseur NK, Bean JF, Philips E, Stein J, Frontera WR, et al. High-intensity resistance training improves muscle strength, self-reported function, and disability in long-term stroke survivors. Stroke. 2004;35(6):1404-9., 1717 Moraes G, Nascimento L, Glória A, Teixeira-Salmela L, Paiva C, Lopes T, et al. A influência do fortalecimento muscular no desempenho motor do membro superior parético de indivíduos acometidos por Acidente Vascular Encefálico. Acta Fisiatr. 2008;15(4):245-8.). Moreover, after the onset of the hemiparesis, stroke subjects demonstrate difficulties in moving and controlling their trunk (1818 Lima N, Rodrigues S, Fillipo T, Oliveira R, Oberg T, Cacho E. Versão brasileira da Escala de Comprometimento do Tronco: um estudo de validade em sujeitos pós-acidente vascular encefálico. Fisioter Pesqui. 2008;15(3):248-53.), which affect their balance, transfer, gait performance, and independence in many daily activities (1515 Karatas M, Çetin N, Bayramoglu M, Dilek A. Trunk muscle strength in relation to balance and functional disability in unihemispheric stroke patients. Am J Phys Med Rehabil. 2004;83(2):81-7.). Thus, the strength of the UL and trunk muscles strength become an important outcome to be evaluated and considered within the clinical decision-making process for the rehabilitation of stroke subjects.

Within clinical settings, the assessment of the strength of the UL and trunk muscles in subjects with stroke is commonly performed with the manual muscle test (MMT). However, due to its subjectivity and the difficulty to evaluate and differ between the degrees of strength rated as good and normal (grades four and five) (1919 Durfee W, Iaizzo P. Rehabilitation and muscle testing. In: Webster J, editor. Encyclopedia of medical devices and instrumentation. 2. ed. Minnesota: Wiley Online Library; 2006., 2020 Wadsworth CT, Krishnan R, Sear M, Harrold J, Nielsen DH. Intrarater reliability of manual muscle testing and hand-held dynametric muscle testing. Phys Ther. 1987;67(9):1342-7.), it is necessary to use more objective and sensitive measures to detect changes in strength, such as the portable and isokinetic dynamometers (1919 Durfee W, Iaizzo P. Rehabilitation and muscle testing. In: Webster J, editor. Encyclopedia of medical devices and instrumentation. 2. ed. Minnesota: Wiley Online Library; 2006.). Portable devices, such as the handheld, handgrip, and pinch dynamometers, are more easily applied within clinical settings, when compared to the isokinetic dynamometer (2121 Sisto S, Dyson-Hudson T. Dynamometry testing in spinal cord injury. J Rehabil Res Dev. 2007;44(1):123-36.).

The portable dynamometers, which record the maximal isometric force generated during an isometric contraction (2222 Morris S, Dodd K, Morris M. Reliability of dynamometry to quantify isometric strength following traumatic brain injury. Brain Inj. 2008;22(13-14):1030-7.), have been used to assess the strength of the trunk (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 2323 Bohannon RW. Interrelationships of trunk and extremity muscle strengths and body awareness following unilateral brain lesions. Percept Mot Skills. 1991; 73(3 Pt 1):1016-8.), UL (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.

26 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3.
-2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30.), and handgrip (9Boissy P, Bourbonnais D, Carlotti MM, Gravel D, Arsenault BA. Maximal grip force in chronic stroke subjects and its relationship to global upper extremity function. Clin Rehabil. 1999;13(4):354-62., 1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94.) and pinch (2929 Conforto A, Kaelin-Lang A, Cohen L. Increase in hand muscle strength of stroke patients after somatosensory stimulation. Ann Neurol. 2002;51(1):122-5.

30 Hummel F, Voller B, Celnik P, Floel A, Giraux P, Gerloff C, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7:73.
-3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70.) muscles of subjects with stroke. They are practical devices that can be placed between the examiner's hand and the muscle group to be tested, similar to the MMT assessment (3232 Andrews AW, Thomas MW, Bohannon RW. Normative values for isometric muscle force measurements obtained with hand-held dynamometers. Phys Ther. 1996;76(3):248-59.) or used with the subject exerting force directly on the equipment, in the case of handgrip and pinch assessments (3333 Figueiredo IM, Sampaio RF, Mancini MC, Silva F, Souza MAP. Teste de força de preensão utilizando o dinamômetro Jamar. Acta Fisiatr. 2007;14(2):104-10.

34 Bohannon RW. Adequacy of hand-grip dynamometry for characterizing upper limb strength after stroke. Isokinet Exerc Sci. 2004;12(4):263-5.

35 Araújo MP, Araújo PMP, Caporrino FA, Faloppa F, Albertoni WM. Estudo populacional das forças das pinças polpa-apolpa, trípode e lateral. Rev Bras Ortop. 2002;37(11-12):496-504.
-3636 Gonçalves GH, Gomes DA, Teixeira MDM, Shimano SGN, Shimano AC, Fonseca MCR. Força de preensão palmar e pinça digital em diferentes grupos de pilotos da Academia da Força Aérea brasileira. Fisioter Pesqui. 2010;17(2):141-6.). Furthermore, they provide quantitative measures of strength, which has an important advantage, compared to the MMT assessment (3737 Stark T, Walker B, Phillips J, Fejer R, Beck R. Hand-held dynamometry correlation with the gold standard isokinetic dynamometry: a systematic review. PM R. 2011;3(5):472-9.).

Studies have reported several factors that could influence the measures obtained with portable dynamometers (2121 Sisto S, Dyson-Hudson T. Dynamometry testing in spinal cord injury. J Rehabil Res Dev. 2007;44(1):123-36., 3333 Figueiredo IM, Sampaio RF, Mancini MC, Silva F, Souza MAP. Teste de força de preensão utilizando o dinamômetro Jamar. Acta Fisiatr. 2007;14(2):104-10.), such as positioning of the subjects and the device, number of repetitions, contraction and rest time, prior demonstration and familiarization with the procedures, and supply of verbal or visual encouragement. Other factors should also be considered when selecting these devices for the assessment of strength in subjects with stroke, such as unilateral or bilateral assessments and the measurement properties already established for this specific population. Before the portable dynamometers be appropriately employed for the measurement of the strength of the UL and trunk muscles of subjects with stroke, it is necessary to standardize the assessment procedures and to ensure that they show appropriate psychometric properties. Within this context, the aims of this study were to investigate whether there were standardized protocols for the use of the portable dynamometers for the assessment of the strength of the UL and trunk muscles, including handgrip and pinch strength, in subjects with stroke, and verify the investigated psychometric properties. Based upon the results of this review, it will be possible to determine the most commonly used protocols and the psychometric properties, to allow a scientifically-based clinical decision making regarding the use of portable dynamometry for the assessment of the UL and trunk muscles in subjects with stroke.

Methods

Initially, electronic searches were performed in MEDLINE (via PUBMED), SciELO, LILACS, and PEDro databases. The MEDLINE search strategy followed guidelines developed by the Cochrane group (3838 Wu H, Tang J, Lin X, Lau J, Leung P, Woo J, et al. Acupuncture for stroke rehabilitation. Cochrane Database Syst Rev. 2006;(3):CD004131.), which was adjusted for the other databases, using descriptors related to UL, trunk, and handheld dynamometry. The search terms used for the UL included words related to handgrip and pinch, were: upper limb, upper extremity, hand grip, palmar grip, grip, grasp, hand strength, pinch, hand, and palmar. For the trunk, the search terms included word related to back, trunk, abdomen, and thorax. Finally, for the dynamometry, the following words were used: Dynamometer, pinch gauge, pinch strength, Preston pinch gauge, Jamar, handheld dynamometer, and muscle strength.

To be included, the studies should clearly report in the methodology section that the strength of the trunk or UL muscles, including handgrip or pinch strength, with portable dynamometers was assessed in subjects with stroke. There were no restrictions regarding the language of publication and all studies published until November 2011 were included.

The selection of the studies was performed by two independent examiners, following three steps, as recommended and commonly used (3939 Moher D, Liberati A, Tetzlaff J, Altman DG; PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg. 2010;8(5):336-41.

40 Puga VOO, Lopes AD, Costa LOP. Avaliação das adaptações transculturais e propriedades de medida de questionários relacionados às disfunções do ombro em língua portuguesa: uma revisão sistemática. Rev Bras Fisioter. 2012;16(2):85-93.
-4141 Faria CDCM, Saliba VA, Teixeira-Salmela LF. Musculoskeletal biomechanics in sit-to-stand and stand-to-sit activities with stroke subjects: a systematic review. Fisioter Mov. 2010; 23(1):35-52.). The first step consisted of reading the titles and excluding the that clearly did not meet the established criteria (3939 Moher D, Liberati A, Tetzlaff J, Altman DG; PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg. 2010;8(5):336-41.

40 Puga VOO, Lopes AD, Costa LOP. Avaliação das adaptações transculturais e propriedades de medida de questionários relacionados às disfunções do ombro em língua portuguesa: uma revisão sistemática. Rev Bras Fisioter. 2012;16(2):85-93.
-4141 Faria CDCM, Saliba VA, Teixeira-Salmela LF. Musculoskeletal biomechanics in sit-to-stand and stand-to-sit activities with stroke subjects: a systematic review. Fisioter Mov. 2010; 23(1):35-52.). Then, the selected abstracts were analyzed and those that did not meet the inclusion criteria were also excluded (3939 Moher D, Liberati A, Tetzlaff J, Altman DG; PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg. 2010;8(5):336-41.

40 Puga VOO, Lopes AD, Costa LOP. Avaliação das adaptações transculturais e propriedades de medida de questionários relacionados às disfunções do ombro em língua portuguesa: uma revisão sistemática. Rev Bras Fisioter. 2012;16(2):85-93.
-4141 Faria CDCM, Saliba VA, Teixeira-Salmela LF. Musculoskeletal biomechanics in sit-to-stand and stand-to-sit activities with stroke subjects: a systematic review. Fisioter Mov. 2010; 23(1):35-52.). The last step consisted of reading the full papers. An active manual search from all selected studies was also performed, following the same previously described criteria and procedures.

Results

The electronic search identified 202 studies. After screening the titles, 122 were excluded for the following reasons: the population was not stroke individuals or the dynamometer was not portable. In the second step, 33 studies were excluded for the same reasons or for not assessing the strength of the trunk or UL muscles. In the third step, eight studies were excluded. Of the 39 studies that met the inclusion criteria, five could not be retrieved. Thus, 34 studies retrieved by the electronic search were included in this review. From the active manual search in these 34 studies, 24 others were included. Therefore, a total of 58 studies fulfilled all eligibility criteria and were included in this review (Figure 1).

Figure 1
Flow chart of the selection of the studies

Amongst the 58 included studies, three evaluated the strength of the trunk (5.17%) (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 2323 Bohannon RW. Interrelationships of trunk and extremity muscle strengths and body awareness following unilateral brain lesions. Percept Mot Skills. 1991; 73(3 Pt 1):1016-8., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.), while 55 (94.83%) analyzed the strength of the UL muscles, including handgrip and pinch strength. Out of the 55, 41 assessed handgrip (4Kamper D, Fischer H, Cruz E, Rymer W. Weakness is the primary contributor to finger impairment in chronic stroke. Arch Phys Med Rehabil. 2006;87(9):1262-9., 9Boissy P, Bourbonnais D, Carlotti MM, Gravel D, Arsenault BA. Maximal grip force in chronic stroke subjects and its relationship to global upper extremity function. Clin Rehabil. 1999;13(4):354-62., 1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 4343 Wade DT, Langton-Hewer R, Wood VA, Skilbeck C, Ismail H. The hemiplegic arm after stroke: measurement and recovery. J Neurol Neurosurg Psychiatry. 1983;46(6):521-4.

44 Kraft G, Fitts S, Hammond M. Techniques to improve function of the arm and hand in chronic hemiplegia. Arch Phys Med Rehabil. 1992;73(3):220-7.

45 Taub E, Miller N, Novack T, Cook III E, Fleming W, Nepomuceno C, et al. Technique to improve chronic motor deficit after stroke. Arch Phys Med Rehabil. 1993;74(4):347-54.

46 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5.

47 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91.

48 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51.

49 Desrosiers J, Bourbounais D, Bravo G, Roy P, Guay M. Performance of the ‘unaffected’ upper extremity of elderly stroke patients. Stroke. 1996;27(9):1564-70.

50 Levy C, Nichols D, Schmalbrock P, Keller P, Chakeres D. Functional MRI evidence of cortical reorganization in upper-limb stroke hemiplegia treated with constraint-induced movement therapy. Am J Phys Med Rehabil. 2001;80(1):4-12.

51 Jack D, Boian R, Merians A, Tremaine M, Burdea G, Adamovich S, et al. Virtual reality-enhanced stroke rehabilitation. IEEE Trans Neural Syst Rehabil Eng. 2001;9(3):308-18.

52 McAniff C, Bohannon RW. Validity of grip strength dynamometry in acute rehabilitation. J PhysTher Sci. 2002;14(1):41-6.

53 Duncan P, Studenski S, Richards L, Gollub S, Lai SM, Reker D, et al. Randomized clinical trial of therapeutic exercise in subacute stroke. Stroke. 2003; 34(9):2173-80.

54 Lang CE, Beebe J. Relating movement control at 9 upper extremity segments to loss of hand function in people with chronic hemiparesis. Neurorehabil Neural Repair. 2007;21(3):279-91.

55 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85.

56 Trickbroom G, Byrnes M, Archer S, Mastaglia F. Motor outcome after subcortical stroke: MEPs correlate with hand strength but not dexterity. Clin Neurophysiol. 2002;113(12):2025-9.

57 Connelly L, Jia Y, Toro M, Stoykov M, Kenyon R, Kamper DG. A pneumatic glove and immersive virtual reality environment for hand rehabilitative training after stroke. IEEE Trans Neural Syst Rehabil Eng. 2010; 18(5):551-9.

58 Triandafilou K, Ochoa J, Kang X, Fischer HC, Stoykov ME, Kamper DG. Transient impact of prolonged versus repetitive stretch on hand motor control in chronic stroke. Top Stroke Rehabil. 2011;18(4):316-24.

59 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53.

60 Jones R, Donaldson I, Parkin P. Impairment and recovery of ipsilateral sensory-motor function following unilateral cerebral infarction. Brain. 1989;112(Pt 1):113-32.

61 van Deusen J, Shalik L, Harlowe D. Construct validation of an acute care occupational therapy cerebral vascular accident assessment tool. Can J Occup Ther. 1990;57(3):155-9.

62 Robinson L, Fitts S, Kraft G. Laterality of performance in fingertapping rate and grip strength by hemisphere of stroke and gender. Arch Phys Med Rehabil. 1990;71(9):695-8.

63 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51.

64 Marque P, Felez A, Puel M, Demonet J, Guiraud-Chaumeil B, Roques C, et al. Impairment and recovery of left motor function in patients with right hemiplegia. J Neurol Neurosurg Psychiatry. 1997;62(1):77-81.

65 Bhakta B, Cozens J, Chamberlain M, Bamford J. Quantifying associated reactions in the paretic arm in stroke and their relationship to spasticity. Clin Rehabil. 2001; 15(2):195-206.

66 Merians A, Jack D, Boian R, Tremaine M, Burdea G, Adamovich S, et al. Virtual reality–augmented rehabilitation for patients following stroke. Phys Ther. 2002;82(9):898-915.

67 Pandyan A, Cameron M, Powell J, Stott D, Granat M. Contractures in the post-stroke wrist: a pilot study of its time course of development and its association with upper limb recovery. Clin Rehabil. 2003;17(1):88-95.

68 Dijkerman H, Ietswaart M, Johnston M, MacWalter R. Does motor imagery training improve hand function in chronic stroke patients? A pilot study. Clin Rehabil. 2004;18(5):538-49.

69 Broeren J, Rydmark M, Sunnerhagen K. Virtual reality and haptics as a training device for movement rehabilitation after stroke: a single-case study. Arch Phys Med Rehabil. 2004;85(8):1247-50.

70 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7.

71 Suputtitada A, Suwanwela N, Tumvitee S. Effectiveness of constraint-induced movement therapy in chronic stroke patients. J Med Assoc Thai. 2004;87(12):1482-90.

72 Wolf SL, Winstein C, Miller J, Taub E, Uswatte G, Morris D, et al. Effect of constraint-induced movement therapy on upper extremity function 3 to 9 months after stroke: the EXCITE randomized clinical trial. JAMA. 2006;296(17):2095-104.

73 Restemeyer C, Weiller C, Liepert J. No effect of a levodopa single dose on motor performance and motor excitability in chronic stroke. A double-blind placebo-controlled cross-over pilot study. Restor Neurol Neurosci. 2007;25(2):143-50.

74 Gosselin S, Desrosiers J, Corriveau H, Hébert R, Rochette A, Provencher V, et al. Outcomes during and after inpatient rehabilitation: comparison between adults and older adults. J Rehabil Med. 2008;40(1):55-60.

75 Kang H, Sok S, Kang J. Effects of meridian acupressure for stroke patients in Korea. J Clin Nurs. 2009; 18(15):2145-52.

76 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103.

77 Bohannon RW. Grip strength impairments among older adults receiving physical therapy in a home-care setting. Percept Mot Skills. 2010;111(3):761-4.
-7878 Burdea G, Cioi D, Martin J, Fensterheim D, Holenski M. The Rutgers Arm II rehabilitation system – a feasibility study. IEEE Trans Neural Syst Rehabil Eng. 2010;18(5):505-14.), 15 pinch (2929 Conforto A, Kaelin-Lang A, Cohen L. Increase in hand muscle strength of stroke patients after somatosensory stimulation. Ann Neurol. 2002;51(1):122-5.

30 Hummel F, Voller B, Celnik P, Floel A, Giraux P, Gerloff C, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7:73.
-3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 4747 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91., 5454 Lang CE, Beebe J. Relating movement control at 9 upper extremity segments to loss of hand function in people with chronic hemiparesis. Neurorehabil Neural Repair. 2007;21(3):279-91., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5757 Connelly L, Jia Y, Toro M, Stoykov M, Kenyon R, Kamper DG. A pneumatic glove and immersive virtual reality environment for hand rehabilitative training after stroke. IEEE Trans Neural Syst Rehabil Eng. 2010; 18(5):551-9., 5858 Triandafilou K, Ochoa J, Kang X, Fischer HC, Stoykov ME, Kamper DG. Transient impact of prolonged versus repetitive stretch on hand motor control in chronic stroke. Top Stroke Rehabil. 2011;18(4):316-24., 6161 van Deusen J, Shalik L, Harlowe D. Construct validation of an acute care occupational therapy cerebral vascular accident assessment tool. Can J Occup Ther. 1990;57(3):155-9., 7171 Suputtitada A, Suwanwela N, Tumvitee S. Effectiveness of constraint-induced movement therapy in chronic stroke patients. J Med Assoc Thai. 2004;87(12):1482-90., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 7878 Burdea G, Cioi D, Martin J, Fensterheim D, Holenski M. The Rutgers Arm II rehabilitation system – a feasibility study. IEEE Trans Neural Syst Rehabil Eng. 2010;18(5):505-14.

79 Lomarev M, Kim D, Richardson S, Voller B, Hallett M. Safety study of high-frequency transcranial magnetic stimulation in patients with chronic stroke. Clin Neurophysiol. 2007;118(9):2072-5.

80 McDonnell M, Hillier S, Miles T, Thompson P, Ridding M. Influence of combined afferent stimulation and task-specific training following stroke: a pilot randomized controlled trial. Neurorehabil Neural Repair. 2007;21(5):435-43.
-8181 Klaiput A, Kitisomprayoonkul W. Increased pinch strength in acute and subacute stroke patients after simultaneous median and ulnar sensory stimulation. Neurorehabil Neural Repair. 2009;23(4):351-6.), and 17 the strength of other UL muscles (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.

26 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3.
-2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5.

47 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91.
-4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.

83 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.

84 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7.

85 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.
-8686 Bohannon RW, Andrews AW. Limb muscle strength is impaired bilaterally after stroke. J Phys Ther Sci. 1995;7(1):1-7.). The studies that measured the strength of the trunk muscles included 59 individuals of both sexes, who had ages ranging from 27 to 87 years and were at the acute stages (three to 27 days post-stroke). Those that assessed handgrip strength included 1,408 individuals of both sexes, who had ages ranging from 16 to 93 years and the time since the onset of stroke ranging from two days to 30 years. The studies which assessed pinch strength included 536 subjects of both sexes, who had ages ranging from 16 to 94 years and the time since the onset of the stroke ranging from two days to 23 years. The studies which evaluated other UL muscles included 468 individuals of both sexes, who had ages ranging from 17 to 89 years and the mean time since the onset of stroke ranging from two days to 30 years.

Regarding the trunk muscles (Table 1), the anterior flexors were evaluated in two studies (66.7%) (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.) and the lateral flexors in all three included studies (100%) (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 2323 Bohannon RW. Interrelationships of trunk and extremity muscle strengths and body awareness following unilateral brain lesions. Percept Mot Skills. 1991; 73(3 Pt 1):1016-8., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.). In all studies, the seated position was used and two reported the data collection protocols, describing the number of trials and the duration of the isometric contractions (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.). One study (33.3%) performed unilateral assessment of the lateral flexors (2323 Bohannon RW. Interrelationships of trunk and extremity muscle strengths and body awareness following unilateral brain lesions. Percept Mot Skills. 1991; 73(3 Pt 1):1016-8.) and two (66.7%) bilateral (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.).

Table 1
Data extraction of the studies which assessed the strength of the trunk muscles in subjects with stroke with portable dynamometers

From the 41 studies that evaluated handgrip strength, 24 (58.54%) provided detailed information regarding the subjects’ positioning or the data collection protocols (Table 2). Since 17 studies did not provide this information (4343 Wade DT, Langton-Hewer R, Wood VA, Skilbeck C, Ismail H. The hemiplegic arm after stroke: measurement and recovery. J Neurol Neurosurg Psychiatry. 1983;46(6):521-4.

44 Kraft G, Fitts S, Hammond M. Techniques to improve function of the arm and hand in chronic hemiplegia. Arch Phys Med Rehabil. 1992;73(3):220-7.

45 Taub E, Miller N, Novack T, Cook III E, Fleming W, Nepomuceno C, et al. Technique to improve chronic motor deficit after stroke. Arch Phys Med Rehabil. 1993;74(4):347-54.

46 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5.

47 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91.

48 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51.

49 Desrosiers J, Bourbounais D, Bravo G, Roy P, Guay M. Performance of the ‘unaffected’ upper extremity of elderly stroke patients. Stroke. 1996;27(9):1564-70.

50 Levy C, Nichols D, Schmalbrock P, Keller P, Chakeres D. Functional MRI evidence of cortical reorganization in upper-limb stroke hemiplegia treated with constraint-induced movement therapy. Am J Phys Med Rehabil. 2001;80(1):4-12.

51 Jack D, Boian R, Merians A, Tremaine M, Burdea G, Adamovich S, et al. Virtual reality-enhanced stroke rehabilitation. IEEE Trans Neural Syst Rehabil Eng. 2001;9(3):308-18.

52 McAniff C, Bohannon RW. Validity of grip strength dynamometry in acute rehabilitation. J PhysTher Sci. 2002;14(1):41-6.

53 Duncan P, Studenski S, Richards L, Gollub S, Lai SM, Reker D, et al. Randomized clinical trial of therapeutic exercise in subacute stroke. Stroke. 2003; 34(9):2173-80.

54 Lang CE, Beebe J. Relating movement control at 9 upper extremity segments to loss of hand function in people with chronic hemiparesis. Neurorehabil Neural Repair. 2007;21(3):279-91.

55 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85.

56 Trickbroom G, Byrnes M, Archer S, Mastaglia F. Motor outcome after subcortical stroke: MEPs correlate with hand strength but not dexterity. Clin Neurophysiol. 2002;113(12):2025-9.

57 Connelly L, Jia Y, Toro M, Stoykov M, Kenyon R, Kamper DG. A pneumatic glove and immersive virtual reality environment for hand rehabilitative training after stroke. IEEE Trans Neural Syst Rehabil Eng. 2010; 18(5):551-9.

58 Triandafilou K, Ochoa J, Kang X, Fischer HC, Stoykov ME, Kamper DG. Transient impact of prolonged versus repetitive stretch on hand motor control in chronic stroke. Top Stroke Rehabil. 2011;18(4):316-24.
-5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53.), they were not included in the table. As can be seen in Table 2, the seated position was employed in 11 studies (73.33%) (9Boissy P, Bourbonnais D, Carlotti MM, Gravel D, Arsenault BA. Maximal grip force in chronic stroke subjects and its relationship to global upper extremity function. Clin Rehabil. 1999;13(4):354-62., 1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 6262 Robinson L, Fitts S, Kraft G. Laterality of performance in fingertapping rate and grip strength by hemisphere of stroke and gender. Arch Phys Med Rehabil. 1990;71(9):695-8., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51., 6565 Bhakta B, Cozens J, Chamberlain M, Bamford J. Quantifying associated reactions in the paretic arm in stroke and their relationship to spasticity. Clin Rehabil. 2001; 15(2):195-206., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 7272 Wolf SL, Winstein C, Miller J, Taub E, Uswatte G, Morris D, et al. Effect of constraint-induced movement therapy on upper extremity function 3 to 9 months after stroke: the EXCITE randomized clinical trial. JAMA. 2006;296(17):2095-104., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 7777 Bohannon RW. Grip strength impairments among older adults receiving physical therapy in a home-care setting. Percept Mot Skills. 2010;111(3):761-4.). Twenty-two studies reported the number of trials and the majority of them performed three trials (72.73%) (9Boissy P, Bourbonnais D, Carlotti MM, Gravel D, Arsenault BA. Maximal grip force in chronic stroke subjects and its relationship to global upper extremity function. Clin Rehabil. 1999;13(4):354-62., 1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 6060 Jones R, Donaldson I, Parkin P. Impairment and recovery of ipsilateral sensory-motor function following unilateral cerebral infarction. Brain. 1989;112(Pt 1):113-32., 6161 van Deusen J, Shalik L, Harlowe D. Construct validation of an acute care occupational therapy cerebral vascular accident assessment tool. Can J Occup Ther. 1990;57(3):155-9., 6464 Marque P, Felez A, Puel M, Demonet J, Guiraud-Chaumeil B, Roques C, et al. Impairment and recovery of left motor function in patients with right hemiplegia. J Neurol Neurosurg Psychiatry. 1997;62(1):77-81., 6565 Bhakta B, Cozens J, Chamberlain M, Bamford J. Quantifying associated reactions in the paretic arm in stroke and their relationship to spasticity. Clin Rehabil. 2001; 15(2):195-206., 6767 Pandyan A, Cameron M, Powell J, Stott D, Granat M. Contractures in the post-stroke wrist: a pilot study of its time course of development and its association with upper limb recovery. Clin Rehabil. 2003;17(1):88-95., 6868 Dijkerman H, Ietswaart M, Johnston M, MacWalter R. Does motor imagery training improve hand function in chronic stroke patients? A pilot study. Clin Rehabil. 2004;18(5):538-49., 7171 Suputtitada A, Suwanwela N, Tumvitee S. Effectiveness of constraint-induced movement therapy in chronic stroke patients. J Med Assoc Thai. 2004;87(12):1482-90.

72 Wolf SL, Winstein C, Miller J, Taub E, Uswatte G, Morris D, et al. Effect of constraint-induced movement therapy on upper extremity function 3 to 9 months after stroke: the EXCITE randomized clinical trial. JAMA. 2006;296(17):2095-104.
-7373 Restemeyer C, Weiller C, Liepert J. No effect of a levodopa single dose on motor performance and motor excitability in chronic stroke. A double-blind placebo-controlled cross-over pilot study. Restor Neurol Neurosci. 2007;25(2):143-50., 7575 Kang H, Sok S, Kang J. Effects of meridian acupressure for stroke patients in Korea. J Clin Nurs. 2009; 18(15):2145-52., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 7878 Burdea G, Cioi D, Martin J, Fensterheim D, Holenski M. The Rutgers Arm II rehabilitation system – a feasibility study. IEEE Trans Neural Syst Rehabil Eng. 2010;18(5):505-14.). The duration of the maximal isometric contractions was reported by five studies, and 10 seconds was the time most commonly used (60%) (2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 6565 Bhakta B, Cozens J, Chamberlain M, Bamford J. Quantifying associated reactions in the paretic arm in stroke and their relationship to spasticity. Clin Rehabil. 2001; 15(2):195-206., 6969 Broeren J, Rydmark M, Sunnerhagen K. Virtual reality and haptics as a training device for movement rehabilitation after stroke: a single-case study. Arch Phys Med Rehabil. 2004;85(8):1247-50.). The resting time was reported in seven studies with alternated measurements between the UL being the most employed method (42.9%) (1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 6868 Dijkerman H, Ietswaart M, Johnston M, MacWalter R. Does motor imagery training improve hand function in chronic stroke patients? A pilot study. Clin Rehabil. 2004;18(5):538-49., 7474 Gosselin S, Desrosiers J, Corriveau H, Hébert R, Rochette A, Provencher V, et al. Outcomes during and after inpatient rehabilitation: comparison between adults and older adults. J Rehabil Med. 2008;40(1):55-60.). Eighteen studies (69.2%) repoted bilateral measures of handgrip strength (4Kamper D, Fischer H, Cruz E, Rymer W. Weakness is the primary contributor to finger impairment in chronic stroke. Arch Phys Med Rehabil. 2006;87(9):1262-9., 9Boissy P, Bourbonnais D, Carlotti MM, Gravel D, Arsenault BA. Maximal grip force in chronic stroke subjects and its relationship to global upper extremity function. Clin Rehabil. 1999;13(4):354-62., 1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 4747 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91., 4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5252 McAniff C, Bohannon RW. Validity of grip strength dynamometry in acute rehabilitation. J PhysTher Sci. 2002;14(1):41-6., 5454 Lang CE, Beebe J. Relating movement control at 9 upper extremity segments to loss of hand function in people with chronic hemiparesis. Neurorehabil Neural Repair. 2007;21(3):279-91.

55 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85.
-5656 Trickbroom G, Byrnes M, Archer S, Mastaglia F. Motor outcome after subcortical stroke: MEPs correlate with hand strength but not dexterity. Clin Neurophysiol. 2002;113(12):2025-9., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 6161 van Deusen J, Shalik L, Harlowe D. Construct validation of an acute care occupational therapy cerebral vascular accident assessment tool. Can J Occup Ther. 1990;57(3):155-9., 6262 Robinson L, Fitts S, Kraft G. Laterality of performance in fingertapping rate and grip strength by hemisphere of stroke and gender. Arch Phys Med Rehabil. 1990;71(9):695-8., 6868 Dijkerman H, Ietswaart M, Johnston M, MacWalter R. Does motor imagery training improve hand function in chronic stroke patients? A pilot study. Clin Rehabil. 2004;18(5):538-49., 7272 Wolf SL, Winstein C, Miller J, Taub E, Uswatte G, Morris D, et al. Effect of constraint-induced movement therapy on upper extremity function 3 to 9 months after stroke: the EXCITE randomized clinical trial. JAMA. 2006;296(17):2095-104., 7474 Gosselin S, Desrosiers J, Corriveau H, Hébert R, Rochette A, Provencher V, et al. Outcomes during and after inpatient rehabilitation: comparison between adults and older adults. J Rehabil Med. 2008;40(1):55-60., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 7777 Bohannon RW. Grip strength impairments among older adults receiving physical therapy in a home-care setting. Percept Mot Skills. 2010;111(3):761-4.), while eight (30.8%) only assessed the paretic limb (3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 4545 Taub E, Miller N, Novack T, Cook III E, Fleming W, Nepomuceno C, et al. Technique to improve chronic motor deficit after stroke. Arch Phys Med Rehabil. 1993;74(4):347-54., 5858 Triandafilou K, Ochoa J, Kang X, Fischer HC, Stoykov ME, Kamper DG. Transient impact of prolonged versus repetitive stretch on hand motor control in chronic stroke. Top Stroke Rehabil. 2011;18(4):316-24., 6464 Marque P, Felez A, Puel M, Demonet J, Guiraud-Chaumeil B, Roques C, et al. Impairment and recovery of left motor function in patients with right hemiplegia. J Neurol Neurosurg Psychiatry. 1997;62(1):77-81., 6565 Bhakta B, Cozens J, Chamberlain M, Bamford J. Quantifying associated reactions in the paretic arm in stroke and their relationship to spasticity. Clin Rehabil. 2001; 15(2):195-206., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 7171 Suputtitada A, Suwanwela N, Tumvitee S. Effectiveness of constraint-induced movement therapy in chronic stroke patients. J Med Assoc Thai. 2004;87(12):1482-90., 7373 Restemeyer C, Weiller C, Liepert J. No effect of a levodopa single dose on motor performance and motor excitability in chronic stroke. A double-blind placebo-controlled cross-over pilot study. Restor Neurol Neurosci. 2007;25(2):143-50.).

Table 2
Data extraction of the 24 studies which assessed handgrip strength in subjects with stroke with portable dynamometers and provided information regarding the subject’ positioning or the data collection protocol

From the 15 studies that assessed pinch strength, lateral pinch was evaluated by nine (2929 Conforto A, Kaelin-Lang A, Cohen L. Increase in hand muscle strength of stroke patients after somatosensory stimulation. Ann Neurol. 2002;51(1):122-5.

30 Hummel F, Voller B, Celnik P, Floel A, Giraux P, Gerloff C, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7:73.
-3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 4747 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91., 5757 Connelly L, Jia Y, Toro M, Stoykov M, Kenyon R, Kamper DG. A pneumatic glove and immersive virtual reality environment for hand rehabilitative training after stroke. IEEE Trans Neural Syst Rehabil Eng. 2010; 18(5):551-9., 5858 Triandafilou K, Ochoa J, Kang X, Fischer HC, Stoykov ME, Kamper DG. Transient impact of prolonged versus repetitive stretch on hand motor control in chronic stroke. Top Stroke Rehabil. 2011;18(4):316-24., 6161 van Deusen J, Shalik L, Harlowe D. Construct validation of an acute care occupational therapy cerebral vascular accident assessment tool. Can J Occup Ther. 1990;57(3):155-9., 7878 Burdea G, Cioi D, Martin J, Fensterheim D, Holenski M. The Rutgers Arm II rehabilitation system – a feasibility study. IEEE Trans Neural Syst Rehabil Eng. 2010;18(5):505-14., 8181 Klaiput A, Kitisomprayoonkul W. Increased pinch strength in acute and subacute stroke patients after simultaneous median and ulnar sensory stimulation. Neurorehabil Neural Repair. 2009;23(4):351-6.), the palmar pinch by seven (4747 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91., 5454 Lang CE, Beebe J. Relating movement control at 9 upper extremity segments to loss of hand function in people with chronic hemiparesis. Neurorehabil Neural Repair. 2007;21(3):279-91., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5757 Connelly L, Jia Y, Toro M, Stoykov M, Kenyon R, Kamper DG. A pneumatic glove and immersive virtual reality environment for hand rehabilitative training after stroke. IEEE Trans Neural Syst Rehabil Eng. 2010; 18(5):551-9., 6161 van Deusen J, Shalik L, Harlowe D. Construct validation of an acute care occupational therapy cerebral vascular accident assessment tool. Can J Occup Ther. 1990;57(3):155-9., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 7878 Burdea G, Cioi D, Martin J, Fensterheim D, Holenski M. The Rutgers Arm II rehabilitation system – a feasibility study. IEEE Trans Neural Syst Rehabil Eng. 2010;18(5):505-14.), pulp-to-pulp pinch by two (7878 Burdea G, Cioi D, Martin J, Fensterheim D, Holenski M. The Rutgers Arm II rehabilitation system – a feasibility study. IEEE Trans Neural Syst Rehabil Eng. 2010;18(5):505-14., 8080 McDonnell M, Hillier S, Miles T, Thompson P, Ridding M. Influence of combined afferent stimulation and task-specific training following stroke: a pilot randomized controlled trial. Neurorehabil Neural Repair. 2007;21(5):435-43.) and tip-to-tip pinch by one (8181 Klaiput A, Kitisomprayoonkul W. Increased pinch strength in acute and subacute stroke patients after simultaneous median and ulnar sensory stimulation. Neurorehabil Neural Repair. 2009;23(4):351-6.). Two studies did not specify the type of pinch that was measured (7171 Suputtitada A, Suwanwela N, Tumvitee S. Effectiveness of constraint-induced movement therapy in chronic stroke patients. J Med Assoc Thai. 2004;87(12):1482-90., 7979 Lomarev M, Kim D, Richardson S, Voller B, Hallett M. Safety study of high-frequency transcranial magnetic stimulation in patients with chronic stroke. Clin Neurophysiol. 2007;118(9):2072-5.). As observed in Table 3, five studies did not provide information regarding the subjects’ positioning or data collection protocols (4747 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91., 5454 Lang CE, Beebe J. Relating movement control at 9 upper extremity segments to loss of hand function in people with chronic hemiparesis. Neurorehabil Neural Repair. 2007;21(3):279-91., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5757 Connelly L, Jia Y, Toro M, Stoykov M, Kenyon R, Kamper DG. A pneumatic glove and immersive virtual reality environment for hand rehabilitative training after stroke. IEEE Trans Neural Syst Rehabil Eng. 2010; 18(5):551-9., 5858 Triandafilou K, Ochoa J, Kang X, Fischer HC, Stoykov ME, Kamper DG. Transient impact of prolonged versus repetitive stretch on hand motor control in chronic stroke. Top Stroke Rehabil. 2011;18(4):316-24.). The seated position was adopted by all four studies that provided information regarding the participants’ positioning (2929 Conforto A, Kaelin-Lang A, Cohen L. Increase in hand muscle strength of stroke patients after somatosensory stimulation. Ann Neurol. 2002;51(1):122-5.

30 Hummel F, Voller B, Celnik P, Floel A, Giraux P, Gerloff C, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7:73.
-3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103.). Ten studies reported the number of trials, and seven used three trials (70%) (3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 6161 van Deusen J, Shalik L, Harlowe D. Construct validation of an acute care occupational therapy cerebral vascular accident assessment tool. Can J Occup Ther. 1990;57(3):155-9., 7171 Suputtitada A, Suwanwela N, Tumvitee S. Effectiveness of constraint-induced movement therapy in chronic stroke patients. J Med Assoc Thai. 2004;87(12):1482-90., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 7878 Burdea G, Cioi D, Martin J, Fensterheim D, Holenski M. The Rutgers Arm II rehabilitation system – a feasibility study. IEEE Trans Neural Syst Rehabil Eng. 2010;18(5):505-14., 8080 McDonnell M, Hillier S, Miles T, Thompson P, Ridding M. Influence of combined afferent stimulation and task-specific training following stroke: a pilot randomized controlled trial. Neurorehabil Neural Repair. 2007;21(5):435-43., 8181 Klaiput A, Kitisomprayoonkul W. Increased pinch strength in acute and subacute stroke patients after simultaneous median and ulnar sensory stimulation. Neurorehabil Neural Repair. 2009;23(4):351-6.). The duration of the contractions was reported by only one study (3030 Hummel F, Voller B, Celnik P, Floel A, Giraux P, Gerloff C, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7:73.), and varied from 1 to 3 seconds. Three studies reported different resting times between the trials: 10s (7979 Lomarev M, Kim D, Richardson S, Voller B, Hallett M. Safety study of high-frequency transcranial magnetic stimulation in patients with chronic stroke. Clin Neurophysiol. 2007;118(9):2072-5.), 15s (8181 Klaiput A, Kitisomprayoonkul W. Increased pinch strength in acute and subacute stroke patients after simultaneous median and ulnar sensory stimulation. Neurorehabil Neural Repair. 2009;23(4):351-6.), and 30s (8080 McDonnell M, Hillier S, Miles T, Thompson P, Ridding M. Influence of combined afferent stimulation and task-specific training following stroke: a pilot randomized controlled trial. Neurorehabil Neural Repair. 2007;21(5):435-43.). Six studies (50%) assessed bilateral pinch strength (4747 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91., 5454 Lang CE, Beebe J. Relating movement control at 9 upper extremity segments to loss of hand function in people with chronic hemiparesis. Neurorehabil Neural Repair. 2007;21(3):279-91., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 6161 van Deusen J, Shalik L, Harlowe D. Construct validation of an acute care occupational therapy cerebral vascular accident assessment tool. Can J Occup Ther. 1990;57(3):155-9., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8080 McDonnell M, Hillier S, Miles T, Thompson P, Ridding M. Influence of combined afferent stimulation and task-specific training following stroke: a pilot randomized controlled trial. Neurorehabil Neural Repair. 2007;21(5):435-43.) and six (50%) only the paretic side (2929 Conforto A, Kaelin-Lang A, Cohen L. Increase in hand muscle strength of stroke patients after somatosensory stimulation. Ann Neurol. 2002;51(1):122-5.

30 Hummel F, Voller B, Celnik P, Floel A, Giraux P, Gerloff C, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7:73.
-3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 5858 Triandafilou K, Ochoa J, Kang X, Fischer HC, Stoykov ME, Kamper DG. Transient impact of prolonged versus repetitive stretch on hand motor control in chronic stroke. Top Stroke Rehabil. 2011;18(4):316-24., 7171 Suputtitada A, Suwanwela N, Tumvitee S. Effectiveness of constraint-induced movement therapy in chronic stroke patients. J Med Assoc Thai. 2004;87(12):1482-90., 8181 Klaiput A, Kitisomprayoonkul W. Increased pinch strength in acute and subacute stroke patients after simultaneous median and ulnar sensory stimulation. Neurorehabil Neural Repair. 2009;23(4):351-6.).

Table 3
Data extraction of the 15 studies which assessed pinch strength in subjects with stroke with portable dynamometers

The main evaluated other muscular groups of the UL (except for handgrip and pinch strength) were the wrist flexors: eight studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5., 4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.); wrist extensors: 13 studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.

26 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3.
-2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5.

47 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91.
-4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94., 8686 Bohannon RW, Andrews AW. Limb muscle strength is impaired bilaterally after stroke. J Phys Ther Sci. 1995;7(1):1-7.); elbow flexors: 17 studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.

26 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3.
-2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5.

47 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91.
-4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.

83 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.

84 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7.

85 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.
-8686 Bohannon RW, Andrews AW. Limb muscle strength is impaired bilaterally after stroke. J Phys Ther Sci. 1995;7(1):1-7.); elbow extensors: ten studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5., 4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.); shoulder flexors: nine studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5.

47 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91.
-4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.); shoulder extensors: eight studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5., 4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.); internal shoulder rotators: five studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.); external shoulder rotators: six studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.
-2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.); and shoulder abductors: nine studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5., 4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8686 Bohannon RW, Andrews AW. Limb muscle strength is impaired bilaterally after stroke. J Phys Ther Sci. 1995;7(1):1-7.). Other muscular groups, such as the shoulder adductors (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.) and flexors (5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103.) and extensors of the index finger (5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103.) were evaluated in two studies.

Of the 17 studies, three did not describe the subjects’ positioning or the data collection protocols (4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5., 4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53.). Fifteen reported the subjects’ positioning and 14 (93.3%) used the supine (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.

26 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3.
-2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 4747 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.

83 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.

84 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7.

85 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.
-8686 Bohannon RW, Andrews AW. Limb muscle strength is impaired bilaterally after stroke. J Phys Ther Sci. 1995;7(1):1-7.) and one (6.7%) the seated position (4747 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91.). Nine studies reported the number of trials and three trials (44.44%) were employed in the majority of the studies (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.). Nine studies described the duration of the maximal isometric contractions and seven (77.8%) used 4 to 5 seconds (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.
-2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8484 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7., 8585 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.). For the rest time, five studies (71.43%) reported 10 to 30 seconds (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.

83 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.
-8484 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7.), and two (28.58%) 1 to 2 minutes between the trials (2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7.). Table 4 shows the data of the studies that examined the strength of other UL muscles, but the three studies that did not describe the subjects’ positioning or data collection protocol were not included. Most studies, 11 (73.3%), performed bilateral measures (2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 4646 Whitall J, McCombe Waller S, Silver K, Macko R. Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Stroke. 2000;31(10):2390-5.

47 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91.
-4848 McCombe Waller S, Whitall J. Hand dominance and side of stroke affect rehabilitation in chronic stroke. Clin Rehabil. 2005;19(5):544-51., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 5959 Stoykov M, Lewis G, Corcos D. Comparison of bilateral and unilateral training for upper extremity hemiparesis in stroke. Neurorehabil Neural Repair. 2009; 23(9):945-53., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94., 8686 Bohannon RW, Andrews AW. Limb muscle strength is impaired bilaterally after stroke. J Phys Ther Sci. 1995;7(1):1-7.) and four (26.7%) unilateral (2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 8484 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7., 8585 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.), three of the paretic hand.

Table 4
Data extraction of the 14 studies which assessed the upper limb strength in subjects with stroke with portable dynamometers and provided information regarding the subject’s positioning or the data collection protocol

Regarding the positioning of the dynamometers, two studies on trunk assessment reported that the device was placed in the lower portion of the jugular notch for the anterior trunk flexors, and in the lateral lower portion of the acromion for the lateral trunk flexors (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.). For the assessment of handgrip strength, the device was positioned between the palm of the hand and the fingers (1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 6565 Bhakta B, Cozens J, Chamberlain M, Bamford J. Quantifying associated reactions in the paretic arm in stroke and their relationship to spasticity. Clin Rehabil. 2001; 15(2):195-206.) with its handle on the second position (7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 7777 Bohannon RW. Grip strength impairments among older adults receiving physical therapy in a home-care setting. Percept Mot Skills. 2010;111(3):761-4.). For the evaluation of pinch strength, the end portion of the device was placed between the thumb and the finger involved in the assessed pinch (2929 Conforto A, Kaelin-Lang A, Cohen L. Increase in hand muscle strength of stroke patients after somatosensory stimulation. Ann Neurol. 2002;51(1):122-5., 3030 Hummel F, Voller B, Celnik P, Floel A, Giraux P, Gerloff C, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7:73., 8181 Klaiput A, Kitisomprayoonkul W. Increased pinch strength in acute and subacute stroke patients after simultaneous median and ulnar sensory stimulation. Neurorehabil Neural Repair. 2009;23(4):351-6.). Studies of other UL muscles reported that the device was positioned perpendicular to the evaluated segment in its distal region, and stabilization was provided to the proximal region (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.

26 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3.
-2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 5555 Beebe J, Lang CE. Absence of a proximal to distal gradient of motor deficits in the upper extremity early after stroke. Clin Neurophysiol. 2008;119(9):2074-85., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.

83 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.

84 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7.
-8585 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.).

Out of the 58 included studies, nine reported the psychometric properties of the portable dynamometers. In these studies, the strength of the trunk (4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.) and some UL muscles (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.
-2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.

84 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7.
-8585 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.), including handgrip (9Boissy P, Bourbonnais D, Carlotti MM, Gravel D, Arsenault BA. Maximal grip force in chronic stroke subjects and its relationship to global upper extremity function. Clin Rehabil. 1999;13(4):354-62., 2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51.), were evaluated, as shown in Table 5. All studies assessed the reliability, five reported test-retest (9Boissy P, Bourbonnais D, Carlotti MM, Gravel D, Arsenault BA. Maximal grip force in chronic stroke subjects and its relationship to global upper extremity function. Clin Rehabil. 1999;13(4):354-62., 2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51.), one intra-rater (8585 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.), two inter-rater (2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.), and one intra- and inter-session reliabilities (8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.). All studies that investigated the psychometric properties of the dynamometer, except one (2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94.), reported the magnitudes of the correlation coefficient values above 0.80, indicating excellent reliability (8787 Portney LG, Watkins MP. Foundations of clinical research: applications to practice. 2. ed. New Jersey: Prentice-Hall; 2000.).

Table 5
Results of the nine studies which assessed the measurement properties of the portable dynamometers

Few studies reported the use of visual or verbal feedback to motivate the participants during the performance of maximal isometric contractions: only two studies that evaluated the strength of the UL muscles (2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 8484 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7.) reported some stimulus. The demonstration and familiarization with the procedures were also rarely reported: four studies related to UL muscles (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.
-2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.), one related to handgrip (2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94.), and one related to pinch strength (8181 Klaiput A, Kitisomprayoonkul W. Increased pinch strength in acute and subacute stroke patients after simultaneous median and ulnar sensory stimulation. Neurorehabil Neural Repair. 2009;23(4):351-6.) reported that demonstration procedures were carried out and familiarization occurred in only one UL study (2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30.) and two of handgrip (2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 6262 Robinson L, Fitts S, Kraft G. Laterality of performance in fingertapping rate and grip strength by hemisphere of stroke and gender. Arch Phys Med Rehabil. 1990;71(9):695-8.).

Discussion

The aim of this study was to investigate whether there were standardized protocols for the use of portable dynamometers for the assessment of strength of the trunk and UL muscles, including handgrip and pinch strength in subjects with stroke, as well as to verify which measurement properties were investigated. The majority of the studies assessed handgrip, followed by elbow flexors, wrist extensors, elbow extensors and lateral pinch strength. In addition, adults and elderly subjects at the acute, sub-acute, and chronic phases after stroke were included, thus covering a large sample variability. Most studies described the positioning of the subjects and/or the data collection protocols, however, without standardized procedures. The only investigated measurement property was reliability, with excellent results in most studies.

The muscular groups of the UL, which were evaluated with portable dynamometry are often impaired in stroke subjects (1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30.) and are important for the performance of functional activities (7Faria-Fortini I, Michaelsen S, Cassiano J, Teixeira-Salmela L. Upper extremity function in stroke subjects: relationships between the International Classification of Functioning, Disability, and Health Domains. J Hand Ther. 2011;24(3):257-65., 5454 Lang CE, Beebe J. Relating movement control at 9 upper extremity segments to loss of hand function in people with chronic hemiparesis. Neurorehabil Neural Repair. 2007;21(3):279-91., 8585 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.). However, despite the extensive search, only three studies related to the strength of the trunk muscles in stroke subjects with portable dynamometry, but they did not include subjects at the chronic phase nor evaluated the strength of the trunk extensor and rotator muscles.

Although weakness of the trunk muscles were already identified in stroke (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51., 8888 Tanaka S, Hachisuska K, Ogata H. Muscle strength of trunk flexion-extension in post-stroke hemiplegic patients. Am J Phys Med Rehabil. 1998;77(4):288-290., 8989 Tanaka S, Hachisuska K, Ogata H. Trunk rotatory muscle performance in post-stroke hemiplegic patients. Am J Phys Med Rehabil. 1997;76(5):366-369.), possibly the strength of the trunk muscles has been poorly evaluated, because the weakness is most remarkable in the upper and lower limb muscles, especially those contralateral to the side of the brain injury (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.). The nerve supply of the trunk muscles provided by both cerebral hemispheres (9090 Taoka M, Toda T, Iwamura Y: Representation of the midline trunk, bilateral arms, and shoulders in the monkey postcentral somatosensory cortex. Exp Brain Res. 1998;123(3):315-22.), which may justify less remarkable impairment of this segment, compared to limbs (1515 Karatas M, Çetin N, Bayramoglu M, Dilek A. Trunk muscle strength in relation to balance and functional disability in unihemispheric stroke patients. Am J Phys Med Rehabil. 2004;83(2):81-7.). Moreover, according to Bohannon (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7.), the recovery of the strength of the trunk muscles follows the time of the onset of stroke (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7.), and therefore, impairments of the trunk muscles are most evident at the acute and sub-acute phases after stroke (1515 Karatas M, Çetin N, Bayramoglu M, Dilek A. Trunk muscle strength in relation to balance and functional disability in unihemispheric stroke patients. Am J Phys Med Rehabil. 2004;83(2):81-7.). In addition, according to Bohannon (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7.), the greatest recovery of strength after stroke was found for the anterior trunk flexors, which is usually the most affected muscular group. Possibly, these are the reasons that the studies that assessed the strength of the trunk muscles included subjects at the acute phases and the assessment of anterior trunk flexors. Within this context, it is important to note that subjects at the chronic phases also demonstrate weakness of the trunk muscles, which is associated with functional limitations (1515 Karatas M, Çetin N, Bayramoglu M, Dilek A. Trunk muscle strength in relation to balance and functional disability in unihemispheric stroke patients. Am J Phys Med Rehabil. 2004;83(2):81-7., 9191 Castellassi CS, Ribeiro EAF, Fonseca VC, Beinotti F, Oberg TD, Lima NMFV. Confiabilidade da versão brasileira da escala de deficiências de tronco em hemiparéticos. Fisioter Mov. 2009;22(2):189-99.). Furthermore, this weakness is observed not only on the anterior trunk flexors, but also on the extensors and rotators (8888 Tanaka S, Hachisuska K, Ogata H. Muscle strength of trunk flexion-extension in post-stroke hemiplegic patients. Am J Phys Med Rehabil. 1998;77(4):288-290., 8989 Tanaka S, Hachisuska K, Ogata H. Trunk rotatory muscle performance in post-stroke hemiplegic patients. Am J Phys Med Rehabil. 1997;76(5):366-369.).

All trunk muscles play an important role in supporting the body during antigravity postures and in stabilizing the proximal body during functional movements of the limbs (9292 Tsuji T, Liu M, Hase K, Masakado Y, Chino N. Trunk muscles in persons with hemiparetic stroke evaluated with computed tomography. J Rehabil Med. 2003; 35(4):184-8.). Adequate function of these muscles is crucial for balance, transfers, gait, and other functional activities (1515 Karatas M, Çetin N, Bayramoglu M, Dilek A. Trunk muscle strength in relation to balance and functional disability in unihemispheric stroke patients. Am J Phys Med Rehabil. 2004;83(2):81-7.), providing stability and mobility for the performance of daily tasks (9393 Aguiar P, Rocha T, Oliveira E. Escalas de controle de tronco como prognóstico funcional em pacientes após acidente vascular encefálico. Acta Fisiatr. 2008; 15(3):160-4.). Therefore, the assessment of the strength of the trunk muscles is essential (1515 Karatas M, Çetin N, Bayramoglu M, Dilek A. Trunk muscle strength in relation to balance and functional disability in unihemispheric stroke patients. Am J Phys Med Rehabil. 2004;83(2):81-7., 9494 Wang C, Hsueh I, Sheu CF, Hsieh CL. Discriminative, predictive, and evaluative properties of a trunk control measure in patients with stroke. Phys Ther. 2005; 85(9):887-94.) for all subjects affected by stroke, because they have significant impairments of these muscles (1515 Karatas M, Çetin N, Bayramoglu M, Dilek A. Trunk muscle strength in relation to balance and functional disability in unihemispheric stroke patients. Am J Phys Med Rehabil. 2004;83(2):81-7., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.).

Despite the widespread use of portable dynamometry for the assessment of UL muscles, including handgrip and pinch strength, only nine studies investigated its measurement properties with stroke subjects. All studies reported data related to reliability, which was found to be excellent in most of them. Test-retest or intra-rater reliability was the most investigated property, probably by the fact that repeated measures by the same examiner are easily obtained, and are commonly used within clinical settings, where the measures of the same professional are compared before and after an intervention, for example. Since the results indicated reliable measures when they are performed by the same examiner, the changes observed in measures performed by the same examiner before and after an intervention, for example, can be attributed to changes obtained with the performed intervention (8787 Portney LG, Watkins MP. Foundations of clinical research: applications to practice. 2. ed. New Jersey: Prentice-Hall; 2000.).

Most of the studies which investigated reliability, calculated the Pearson correlation coefficients to correlate the measurements obtained in different sessions (defined by the authors as intra-rater or test-retest reliability) or by different examiners (inter-rater reliability). However, this statistical test only evaluates the degree of associations between the measures, without considering the levels of agreement and, therefore, it is not considered the most adequate method for the assessment of reliability (8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94., 8787 Portney LG, Watkins MP. Foundations of clinical research: applications to practice. 2. ed. New Jersey: Prentice-Hall; 2000.). On the other hand, intra-class correlation coefficients (ICCs) are mostly recommended to assess reliability, since they reflect both the associations and the agreement between two or more measures (8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94., 8787 Portney LG, Watkins MP. Foundations of clinical research: applications to practice. 2. ed. New Jersey: Prentice-Hall; 2000.). All four studies that used ICCS, reported coefficients 0.80, which are indicative of excellent reliability.

Another important issue to be considered is that the terminology used in the studies to specify the types of similar reliability varied: test-retest, intra-, inter-session, and intra-rater reliability. Test-retest reliability is used to determine whether an instrument or test provides consistent measures, keeping all other measurement conditions as constant, as possible (8787 Portney LG, Watkins MP. Foundations of clinical research: applications to practice. 2. ed. New Jersey: Prentice-Hall; 2000.). In the case of portable dynamometry assessment, in which the resistance exerted by the examiners is critical, it is necessary to guarantee that their measures are reliable. As pointed out by Portney and Watkins (8787 Portney LG, Watkins MP. Foundations of clinical research: applications to practice. 2. ed. New Jersey: Prentice-Hall; 2000.), “in a test-retest situation, when a rater’s skill is relevant to the accuracy of the test, intra-rater reliability and test-retest reliability are essentially the same estimate. The effects of rater and the test cannot be separated out”.

The results of this review found that validity was not investigated for portable dynamometer with stroke subjects. Despite the fact that portable dynamometers are devices with adequate face validity for the measurement of strength, studies were found that compared the measurements provided by the portable dynamometers with those obtained with isokinetic dynamometers, which are considered the gold standard for the assessment of strength (3737 Stark T, Walker B, Phillips J, Fejer R, Beck R. Hand-held dynamometry correlation with the gold standard isokinetic dynamometry: a systematic review. PM R. 2011;3(5):472-9.). These studies, which evaluated various muscular groups and subjects with different health conditions, reported good concurrent criterion-related validity for the portable dynamometry. However, they did not assessed the strength of the UL and trunk muscles nor stroke subjects (3737 Stark T, Walker B, Phillips J, Fejer R, Beck R. Hand-held dynamometry correlation with the gold standard isokinetic dynamometry: a systematic review. PM R. 2011;3(5):472-9.). Considering that the subjects’ characteristics could influence the measurements obtained with these devices, such as difficulty in understanding the commands (2World Health Organization. Neurological disorders: public health challenges. Geneva: WHO Library Cateloguin-in-Publication Data; 2006.) and recruiting motor units for the generation of strength (9595 Ng SSM, Shepherd RB. Weakness in patients with stroke: implications for strength training in neurorehabilitation. Phys Ther Rev. 2000;5(4):227-38.), it becomes necessary to investigate the concurrent criterion-related validity of the portable dynamometry for the assessment of these muscular groups with this population.

Amongst the muscular groups commonly evaluated with portable dynamometers in stroke subjects, the measurement properties of the pinch strength were not investigated. According to Araújo et al. (3535 Araújo MP, Araújo PMP, Caporrino FA, Faloppa F, Albertoni WM. Estudo populacional das forças das pinças polpa-apolpa, trípode e lateral. Rev Bras Ortop. 2002;37(11-12):496-504.), pinch strength measures are related to dexterity and accuracy of the movements. Faria-Fortini et al. (7Faria-Fortini I, Michaelsen S, Cassiano J, Teixeira-Salmela L. Upper extremity function in stroke subjects: relationships between the International Classification of Functioning, Disability, and Health Domains. J Hand Ther. 2011;24(3):257-65.) found that impairments of the lateral pinch strength in subjects with stroke were associated with deficits in functional activities. Thus, the measurement properties of the portable dynamometers for the assessment of strength in this population should be investigated. To recommend the use of an instrument in a given population, such as stroke subjects, for the assessment of a specific muscular group, it is necessary that its measurement properties be established, considering the context of interest, such as the population and/or muscular groups, for example. The validity and reliability of a method and/or a measurement instrument is not guaranteed if they are used within contexts, which are different from those for which they were developed (8787 Portney LG, Watkins MP. Foundations of clinical research: applications to practice. 2. ed. New Jersey: Prentice-Hall; 2000., 9696 Streiner DL, Norman GR. Health measurment scales: a pratical guide do their development and use. 4. ed. New York: Oxford; 2008.).

Most of the studies performed bilateral measures of the strength of the UL, including handgrip strength. The loss of strength of the paretic side is a common impairment in stroke subjects. However, weakness is also commonly observed on the non-paretic side (6060 Jones R, Donaldson I, Parkin P. Impairment and recovery of ipsilateral sensory-motor function following unilateral cerebral infarction. Brain. 1989;112(Pt 1):113-32., 8686 Bohannon RW, Andrews AW. Limb muscle strength is impaired bilaterally after stroke. J Phys Ther Sci. 1995;7(1):1-7.). Due to the decrease in overall strength in subjects affected by stroke, it is necessary that these measures are obtained bilaterally (8686 Bohannon RW, Andrews AW. Limb muscle strength is impaired bilaterally after stroke. J Phys Ther Sci. 1995;7(1):1-7., 9797 Andrews AW, Bohannon RW. Distribution of muscle strength impairments following stroke. Clin Rehabil. 2000;14(1):79-87.).

The positioning for the assessment of handgrip and pinch strength, in most studies, followed the recommendation of the American Society of Hand Therapists, with the participant seated, shoulder adducted, elbow flexed to 90°, forearm in neutral position, wrist between 0° and 30° of extension, and 0°and 15° of ulnar deviation (2929 Conforto A, Kaelin-Lang A, Cohen L. Increase in hand muscle strength of stroke patients after somatosensory stimulation. Ann Neurol. 2002;51(1):122-5.

30 Hummel F, Voller B, Celnik P, Floel A, Giraux P, Gerloff C, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7:73.
-3131 Ploughman M, Shears J, Hutchings L, Osmond M. Constraint-induced movement therapy for severe upper-extremity impairment after stroke in an outpatient rehabilitation setting: a case report. Physiother Can. 2008;60(2):161-70., 6363 Bohannon RW. Consistency of paretic upper extremity motor performance soon after stroke. J Phys Ther Sci. 1995;7(2):49-51., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 7272 Wolf SL, Winstein C, Miller J, Taub E, Uswatte G, Morris D, et al. Effect of constraint-induced movement therapy on upper extremity function 3 to 9 months after stroke: the EXCITE randomized clinical trial. JAMA. 2006;296(17):2095-104., 7676 Beebe J, Lang CE. Relationships and responsiveness of six upper extremity function tests during the first six months of recovery after stroke. J Neurol Phys Ther. 2009;33(2):96-103., 7777 Bohannon RW. Grip strength impairments among older adults receiving physical therapy in a home-care setting. Percept Mot Skills. 2010;111(3):761-4.). Most studies that evaluated the trunk muscles, handgrip, and pinch strength adopted the sitting position, while the supine position was further used to evaluate the muscles of the other UL muscles. Most studies that evaluated the strength of other UL muscles placed the limb in a position to avoid the influence of the gravity. The MMT, which is the most common method for the assessment of strength within clinical settings usually follows the position recommended by Kendall et al. (9898 Kendall FP, McCreary EK, Provance PG, Rodgers MM, Romani WA. Músculos: provas e funções. 5. ed. Barueri: Manole; 2007.). Only one study (4747 Byl N, Roderick J, Mohamed O, Hanny M, Kotler J, Smith A, et al. Effectiveness of sensory and motor rehabilitation of the upper limb following the principles of neuroplasticity: patients stable poststroke. Neurorehabil Neural Repair. 2003;17(3):176-91.) cited the same position described by Kendall et al. (9898 Kendall FP, McCreary EK, Provance PG, Rodgers MM, Romani WA. Músculos: provas e funções. 5. ed. Barueri: Manole; 2007.) and did not avoid the influence of gravity to test the strength of the UL muscles. For the assessment of the trunk and UL muscles, the equipment was positioned perpendicular to the evaluated segment and in the case of the UL, in the distal extremity.

The contraction time, which was most used for the UL muscles varied from 4 to 5 seconds (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.
-2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8484 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7., 8585 Bohannon RW, Warren M, Cogman K. Motor variables correlated with the hand-to-mouth maneuver in stroke patients. Arch Phys Med Rehabil. 1991;72(9):682-4.); for the handgrip strength, it was about 10 seconds (2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 6565 Bhakta B, Cozens J, Chamberlain M, Bamford J. Quantifying associated reactions in the paretic arm in stroke and their relationship to spasticity. Clin Rehabil. 2001; 15(2):195-206., 6969 Broeren J, Rydmark M, Sunnerhagen K. Virtual reality and haptics as a training device for movement rehabilitation after stroke: a single-case study. Arch Phys Med Rehabil. 2004;85(8):1247-50.). Only one study regarding pinch strength described contraction time of 1 to 3 seconds (3030 Hummel F, Voller B, Celnik P, Floel A, Giraux P, Gerloff C, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7:73.), and for the trunk muscles, this time ranged from 3 to 5 seconds (1414 Bohannon RW. Recovery and correlates of trunk muscle strength after stroke. Int J Rehabil Res. 1995; 18(2):162-7., 4242 Bohannon RW, Cassidy D, Walsh S. Trunk muscle strength is impaired multidirectionally after stroke. Clin Rehabil. 1995;9(1):47-51.). The time of maximum effort was also quite varied. However, most of the studies included in this review used 4 to 5 seconds, whose values can be used as references.

The rest interval also varied between the studies. The most widely used for the UL muscles was 10 to 30 seconds (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.) and for the handgrip strength was the alternate method (1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 6868 Dijkerman H, Ietswaart M, Johnston M, MacWalter R. Does motor imagery training improve hand function in chronic stroke patients? A pilot study. Clin Rehabil. 2004;18(5):538-49., 7474 Gosselin S, Desrosiers J, Corriveau H, Hébert R, Rochette A, Provencher V, et al. Outcomes during and after inpatient rehabilitation: comparison between adults and older adults. J Rehabil Med. 2008;40(1):55-60.). Mathiowetz (9999 Mathiowetz V. Effects of three trials on grip and pinch strength measurements. J Hand Ther. 1990;3(4):195-8.) reported that it is not really necessary to extend the rest interval, because the differences between measurements with different rest interval are small. Trossman et al. (100100 Trossman P, Li P. The effect of the duration of intertrial rest periods on isometric grip strength performance in young adults. Occup Ther J Res. 1989;9(6):362-78.) investigated the effect of rest interval between five trials and did not found significant differences between rest intervals of 60s, 30s, and 15s. Therefore, rest intervals of 15s seem to be sufficient to avoid effects of fatigue.

The scoring method most commonly used to analyze the maximal isometric strength in stroke subjects was the mean of three trials (9Boissy P, Bourbonnais D, Carlotti MM, Gravel D, Arsenault BA. Maximal grip force in chronic stroke subjects and its relationship to global upper extremity function. Clin Rehabil. 1999;13(4):354-62., 1212 Sunderland A, Tinson D, Bradley L, Hewer R. Arm function after stroke. An evaluation of grip strength as a measure of recovery and a prognostic indicator. J Neurol Neurosurg Psychiatry. 1989;52(11):1267-72., 2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9., 2525 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5., 6060 Jones R, Donaldson I, Parkin P. Impairment and recovery of ipsilateral sensory-motor function following unilateral cerebral infarction. Brain. 1989;112(Pt 1):113-32., 6161 van Deusen J, Shalik L, Harlowe D. Construct validation of an acute care occupational therapy cerebral vascular accident assessment tool. Can J Occup Ther. 1990;57(3):155-9., 6565 Bhakta B, Cozens J, Chamberlain M, Bamford J. Quantifying associated reactions in the paretic arm in stroke and their relationship to spasticity. Clin Rehabil. 2001; 15(2):195-206., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.). Variations of the scoring were reported in healthy subjects, for example, the use of only one trial, the best value of two or three trials (101101 Coldham F, Lewis J, Lee H. The reliability of one vs. three grip trials in symptomatic and asymptomatic subjects. J Hand Ther. 2006;19(3):318-26.). Coldham et al. (101101 Coldham F, Lewis J, Lee H. The reliability of one vs. three grip trials in symptomatic and asymptomatic subjects. J Hand Ther. 2006;19(3):318-26.) evaluated handgrip strength in healthy subjects and in subjects who had undergone orthopedic surgery, and reported that the use of only one trial of maximum strength was appropriate, less painful, and as reliable as the mean or the best value of three trials. Similar studies in subjects with stroke are needed to determine if the mean of three trials is the best scoring method. However, none of the studies included in this review compared different ways of scoring the measures provided by portable dynamometer (mean of two or three trials, or the value of a single trial).

Few studies reported procedures of demonstration (2424 Bohannon RW. Test-retest reliability of hand-held dynamometry during a single session of strength assessment. Phys Ther. 1986;66(2):206-9.

25 Bohannon RW, Smith MB. Assessment of strength deficits in eight paretic upper extremity muscle groups of stroke patients with hemiplegia. Phys Ther. 1987; 67(4):522-5.
-2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 8181 Klaiput A, Kitisomprayoonkul W. Increased pinch strength in acute and subacute stroke patients after simultaneous median and ulnar sensory stimulation. Neurorehabil Neural Repair. 2009;23(4):351-6., 8282 Bohannon RW, Smith MB. Upper extremity strength deficits in hemiplegic stroke patients: relationship between admission and discharge assessment and time since onset. Arch Phys Med Rehabil. 1987;68(3):155-7.) and familiarization with the devices and/or with the data collection protocol (2727 Andrews AW, Bohannon RW. Short-term recovery of limb muscle strength after acute stroke. Arch Phys Med Rehabil. 2003;84(1):125-30., 2828 Hammer A, Lindmark B. Test-retest intra-rater reliability of grip force in patients with stroke. J Rehabil Med. 2003;35(4):189-94., 6262 Robinson L, Fitts S, Kraft G. Laterality of performance in fingertapping rate and grip strength by hemisphere of stroke and gender. Arch Phys Med Rehabil. 1990;71(9):695-8.) or provided stimulation for motivating the participants (2626 Bohannon RW, Andrews AW. Interrater reliability of hand-held dynamometry. Phys Ther. 1987; 67(6):931-3., 8484 Bohannon RW, Andrews AW. Influence of head-neck rotation on static elbow flexion force of paretic side in patients with hemiparesis. Phys Ther. 1989; 69(2):135-7.) during data collection. These factors may influence the measurements of strength obtained with portable dynamometry. Consistent instructions for performing a standardized protocol could minimize the errors and promote better quality of the measures (3333 Figueiredo IM, Sampaio RF, Mancini MC, Silva F, Souza MAP. Teste de força de preensão utilizando o dinamômetro Jamar. Acta Fisiatr. 2007;14(2):104-10., 102102 Innes E. Handgrip strength testing: a review of the literature. Aust OccupTher J. 1999;46(3):120-4.). Considering stroke subjects, who show difficulties in achieving contractions, especially on the paretic side (7070 Bohannon RW. Adequacy of simple measures for characterizing impairment in upper limb strength following stroke. Percept Mot Skills. 2004;99(3 Pt 1):813-7., 8383 Riddle D, Finucane S, Rothstein J, Walker M. Intrasession and intercession reliability of hand-held dynamometer measurements taken on brain-damaged patients. Phys Ther. 1989;69(3):182-94.) and in understanding (2World Health Organization. Neurological disorders: public health challenges. Geneva: WHO Library Cateloguin-in-Publication Data; 2006.), procedures related to demonstration, familiarization, and encouragement are essential to obtain adequate measures of strength.

Final considerations

Portable dynamometry has been used for the assessment of most muscular groups of the UL in stroke subjects, including handgrip and pinch strength, with large and varied samples. However, the same was not observed for the muscles of the trunk. Most studies provided some information regarding the subjects’ positioning and/or data collection protocol, however, without any standardization. Few studies investigated the measurement properties of the portable dynamometer and only reliability was reported, with adequate results in most of the studies. Few studies have reported procedures related to familiarization and/or motivation. No studies were found which investigated the reliability of portable dynamometer for the assessment of pinch strength, neither its validity in subjects with stroke. Thus, there are still important gaps that limit adequate scientific foundation for the clinical decision making regarding the use of portable dynamometer for the assessment of the strength of the UL and trunk muscles in individuals with stroke.

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Publication Dates

  • Publication in this collection
    Mar 2015

History

  • Received
    23 Oct 2013
  • Accepted
    09 Apr 2014
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