A randomized clinical trial on the effects of remote intercessory prayer in the adverse outcomes of pregnancies

Ensaio clínico randomizado sobre os efeitos da oração intercessória nos desfechos adversos da gestação

Abstracts

The scope of this article was to investigate whether intercessory prayer (IP) influences the adverse outcomes of pregnancies. A double-blind, randomized clinical trial was conducted with 564 pregnant women attending a prenatal public health care service. The women were randomly assigned to an IP group or to a control group (n = 289 per group). They were simultaneously and randomly assigned to practice prayer off-site or not. The following parameters were evaluated: Apgar scores, type of delivery and birth weight. The mean age of the women was 25.1 years of age (± 7.4), and the average gestational age was 23.4 weeks (± 8.1). The average number of years of schooling for the women was 8.1 years (± 3.1). The women in the IP and control groups presented a similar number of adverse medical events with non-significant p. No significant differences were detected in the frequency of adverse outcomes in pregnant women who practiced IP and those in the control group.

Intercessory prayer; Randomized clinical trial; Pregnant women; Excess birth weight; Apgar scores; Birth weight


Este artigo tem por objetivo investigar se a oração intercessória influencia os desfechos adversos das mulheres grávidas. Foi realizado ensaio clínico randomizado duplo-cego com uma população de 564 gestantes que frequentavam Serviço de pré-natal de serviço público de saúde. As gestantes foram aleatoriamente designadas para grupo de intercessão ou grupo controle (n = 289 por grupo). Foram avaliados os seguintes parâmetros: índice de Apgar, tipo de parto, peso ao nascer. A idade média das mulheres foi de 25,1 anos (±7,4) e a idade gestacional média foi de 23,4 semanas (± 8,1). A média de anos de escolaridade foi de 8,1 anos (± 3,1). As mulheres que receberam intervenção (Oração intercessória) e grupo controle exibiram um número similar de eventos adversos, com p não significativo. Não encontramos diferença significativa entre os desfechos adversos na gestação entre os grupos que receberam oração intercessória e no grupo controle.

Oração intercessória; Ensaio clínico randomizado; Gestantes; Macrossomia; Apgar; Baixo peso


ARTICLE ARTIGO

A randomized clinical trial on the effects of remote intercessory prayer in the adverse outcomes of pregnancies

Ensaio clínico randomizado sobre os efeitos da oração intercessória nos desfechos adversos da gestação

Maria Inês da RosaI; Fabio Rosa SilvaI; Bruno Rosa SilvaI; Luciana Carvalho CostaI; Angela Mendes BergamoI; Napoleão Chiaramonte SilvaI; Lidia Rosi de Freitas MedeirosI; Iara Denise Endruweit BattistiII; Rafael AzevedoI

ILaboratório de Epidemiologia, Universidade do Extremo Sul Catarinense. Av. Universitária 1105, Pinheirinho. 88.806-000 Criciuma SC. mir@unesc.net

IIUniversidade Fronteira Sul

ABSTRACT

The scope of this article was to investigate whether intercessory prayer (IP) influences the adverse outcomes of pregnancies. A double-blind, randomized clinical trial was conducted with 564 pregnant women attending a prenatal public health care service. The women were randomly assigned to an IP group or to a control group (n = 289 per group). They were simultaneously and randomly assigned to practice prayer off-site or not. The following parameters were evaluated: Apgar scores, type of delivery and birth weight. The mean age of the women was 25.1 years of age (± 7.4), and the average gestational age was 23.4 weeks (± 8.1). The average number of years of schooling for the women was 8.1 years (± 3.1). The women in the IP and control groups presented a similar number of adverse medical events with non-significant p. No significant differences were detected in the frequency of adverse outcomes in pregnant women who practiced IP and those in the control group.

Key words Intercessory prayer, Randomized clinical trial, Pregnant women, Excess birth weight, Apgar scores, Birth weight

RESUMO

Este artigo tem por objetivo investigar se a oração intercessória influencia os desfechos adversos das mulheres grávidas. Foi realizado ensaio clínico randomizado duplo-cego com uma população de 564 gestantes que frequentavam Serviço de pré-natal de serviço público de saúde. As gestantes foram aleatoriamente designadas para grupo de intercessão ou grupo controle (n = 289 por grupo). Foram avaliados os seguintes parâmetros: índice de Apgar, tipo de parto, peso ao nascer. A idade média das mulheres foi de 25,1 anos (±7,4) e a idade gestacional média foi de 23,4 semanas (± 8,1). A média de anos de escolaridade foi de 8,1 anos (± 3,1). As mulheres que receberam intervenção (Oração intercessória) e grupo controle exibiram um número similar de eventos adversos, com p não significativo. Não encontramos diferença significativa entre os desfechos adversos na gestação entre os grupos que receberam oração intercessória e no grupo controle.

Palavras-chave Oração intercessória, Ensaio clínico randomizado, Gestantes, Macrossomia, Apgar, Baixo peso

Introduction

Praying for help and healing is a fundamental practice in most societies; however, the object to which these prayers are directed varies among the religions in the world1. Ninety five percent of Americans claim to believe in God, and 58% report that religion forms is a very important part of their lives2.Many Americans also use religious activity to cope with stressful life events, such as, a diagnosis of cancer3. Although religion is important to many patients, physicians tend to ignore the religious beliefs of their patients when taking care of them4.

In 2001, the US National Center for Complementary and Alternative Medicine defined "frontier medicine" as a group of therapies "for which there is no plausible biomedical explanation"5. There are many different forms of prayer, such as, organized prayer to God according to an advanced belief system, individual sporadic prayer, spiritual healing, meditation and thanksgiving. Prayers can be spoken from within the framework of a variety of faiths and also by individuals who do not ascribe to a particular, formalized belief system.

Many studies claim to have demonstrated the effectiveness of intercessory prayer(IP) in improving disease6,7. Byrd6 measured the efficacy of IP in curing diseases. They found that 14% of the subjects who practiced IP and 22% of the subjects in the control group had a poor outcome during hospitalization, and this difference was statistically significant.

However, many of these claims are not adequately supported. One meta-analysis of 14 controlled studies concluded that there is no scientifically discernible treatment effect for IP8. Additional reports in the literature are inconclusive, and the general consensus in the field is that the current evidence is compelling enough to warrant further investigation. Although the results of individual studies suggest a positive treatment effect of IP, most of the studies do not support this claim because the evidence does not support a recommendation either in favor or against practicing IP9. Therefore, the aim of this study was to investigate whether IP had an effect on the adverse outcomes of a group of pregnant women.

Methods

Trial design

We conducted a double blind, randomized controlled trial with 564 pregnant women attending a prenatal care public health service clinic between February 2008 and December 2008. The study was approved by the University of Extremo Sul Catarinense Ethics Committee. All participants signed an informed consent.

Participants

Pregnant women (578) were enrolled into the study. The exclusion factor was being pregnant for over 37 weeks because of the proximity of the delivery could not do the intervention on time.

Intervention

A group of six women, who were selected to pray for nine consecutive days, the same pray for all pregnant women from the intervention group. The group of women who practiced IP was coordinated by a theologian, who led a prayer asking for a good delivery and a healthy newborn.

Outcomes

The outcomes analyzed were as follows: type of delivery, Apgar scores, birth weight and macrossomy. The independent variables analyzed were: age, length of gestation, associated diseases, belief in God and religion. All variables were dichotomized.

Sample size

Based on Byrd's study6 we evaluated the table that represents the calculation for the different proportions using the chi-square test to compare the proportions of dichotomous variables10. Based on this evaluation, we found that, considering a bidirectional alpha = 0.05 and beta = 0.20, the difference between the proportions was 10%, for a total number of 289 women per group. In this study 578 pregnant women were enrolled at baseline.

Randomization

All the interviews for the enrollment of the subjects into the study were performed by one of two staff members, who assigned enrollment numbers to the subjects. After enrollment was complete, a staff member used a random number table to assign study codes to each of the subjects' enrollment numbers. These codes were then randomized by a computer. Only this researcher had knowledge of who was in the treated group, and control group and this research was who contacted the coordinator of the group of intercessors providing the first name of the pregnant woman. The patients were then simultaneously and randomly assigned to practice or not to practice prayer off-site. Half of the patients were randomly assigned to the IP group, and the other half was assigned to the control group (n = 289 per group).

Blinding

This study was double blind. None pregnant woman knew if would receive intercessory prayer or not. There searcher also had no knowledge of who was the group that received the intervention and who did not. The IP group coordinator was blinded to the identity of the subjects, with only the subjects' first name being provided.

Statistical analysis

The baseline continuous variables were compared using the Student t-test. The baseline and outcome categorical variables were compared using the chi-square test. Risk ratios and 95% CIs were used for the comparison of the groups. A Poisson robust regression model was used to evaluate whether baseline covariates, were associated with the occurrence of complications in the delivery and to assess the consistency of the unadjusted and final models. Pre-specified covariates were included in model, and variables with P-values of less than 0.05 were retained in the final models. Statistical analyses were performed using STATA version 9 software.

Results

Eight pregnant women from the IP group and five from the control group were lost during follow-up. Therefore, our final analysis included 281 pregnant women from the IP group and 285 pregnant women from the control group (Figure1).

The mean age of the women was 25.1 years old (± 7.4), and the average gestational age was 23.4 weeks (± 8.1). The average years of schooling for the women was 8.1 years (± 3.1). As shown in Table 1, the two groups of women had similar baseline characteristics. The only difference between the groups was the number of abortions that they had previously undergone (P = 0.007).

Both groups of women had a similar number of serious medical adverse events, including spontaneous abortion (p = 0.53), intrauterine death and stillbirth (p = 0.30), low Apgar score (p = 0.34), preterm birth (p = 0.33), small size for gestational age (p = 0.62), macrossomy (p = 0.09), cesarean delivery (p = 0.68) and malformation (p = 0.99) (Table 2).

Discussion

Distant IP appears to have no significant effect on the outcome of pregnant women. This rigorously designed blind, randomized controlled trial conducted with pregnant women showed no significant effect in adverse outcomes of distant IP. However, there are numerous challenges when designing and conducting a study of IP. First, because there is no accepted scientific basis for the effects of IP on illness, it is very difficult to select a biologically relevant patient outcome to study in a clinical trial. Also, the selected outcome may not be associated with the effects of IP, making it difficult to interpret the results of such a study. Second, the duration of IP that should be practiced to observe an effect is not known, which is due, in part, to the lack of a biological basis for the effects of IP. Investigations of the potential therapeutic effects of IP have been conducted on a variety of health areas including: cardiology6,11,12,diabetes13, alcoholism14, mental health15, arthritis16, infections17 and fertility18. Additionally, because the type of IP practiced in a study may be inadequate to evaluate the outcome of the studies, the lack of an effect could be due to inadequate treatment. Similarly, while it may be appealing to suggest that there is a dose-dependent relationship between IP and outcome, the lack of a known mechanism for the effects of IP prevent us from conducting such an analysis. Third, because it is impossible (and not desirable) to limit the prayer practiced by family, friends and others, a study of IP can only evaluate the effects of additional IP, not the effects of prayer in general. Also, the intervention (intercessory prayer) only includes the IP provided by the intercessors, not the effect or result of communication with God. Fourth, documentation of how and when IP is practiced and the inclusion of a specific intention may interfere with the usual practice of the intercessors. The IP practiced during a clinical trial may be different from the IP usually conducted by the intercessors, limiting the interpretation of the results. Given these challenges, it is not surprising that previous studies of IP are controversial18,19.

Only a few clinical trials have found an association between remote prayer and adverse outcomes (generally defined as intermediate clinical endpoints, self-reported health status, morbidity or mortality). In a trial of 393 coronary care unit (CCU) patients, Byrd6 found a statistically significant positive effect between Christian prayer "to a Judeo-Christian God" and six out of 26 outcome variables, as well as with a global hospital course score. Harris et al.11 replicated Byrd's findings, finding no effect on 31 additional clinical variables. However, Harris et al.11 developed a CCU course score specific to their study, which improved significantly (by 10%) in the subjects who prayed.

A recent systematic review of the literature described multiple randomized trials in which other interventions versus personal, focused, committed and organized IP (guided by intercessors holding some belief that they are praying to God or a god) were compared. The review described prayer that was offered on behalf of anyone with health problems and included ten studies (7646 total patients). A comparison of IP plus standard care versus standard care alone revealed that there was no clear effect of IP on death; the effect of IP on death was not statistically significant, and the data were heterogeneous [6 randomized controlled trials (RCTs), n = 6784, random-effects, RR: 0.77, CI: 0.51 to 1.16, I2: 83%]. Additionally, there was no significant difference between the groups with respect to their general clinical state (5 RCTs, n = 2705, RR intermediate or bad outcome: 0.98, CI: 0.86 to 1.11). Four studies found no effect of IP on re-admission to the CCU (4 RCTs, n = 2644, RR: 1.00, CI: 0.77 to 1.30), and two other trials found that IP had no effect on re-hospitalization rate (2 RCTs, n = 1155, RR: 0.93, CI: 0.71 to 1.22). Overall, the review concluded that, although the findings are equivocal and some of the results suggest a positive treatment effect of IP, most studies do not reach this conclusion, and the evidence does not support a recommendation either for or against the use of IP. We are not convinced that further trials of IP should be undertaken and rather suggest that any resources available for such a trial should be used to investigate other questions in healthcare9. Jørgensen et al.20 made a critical analysis of the above mentioned systematic review saying that, "this Cochrane Reviews article, which evaluates a mixture of theological and scientific arguments, is unsound and unhelpful and would, if accepted, make all scientific endeavors meaningless. The review fails badly to live up to the high standards required for Cochrane Reviews, and we therefore suggest it be withdrawn". Our negative findings do not imply that therapeutic relationships and positive therapeutic intent do not have beneficial treatment effects for individual patients. Rather, we suggest that additionally studies using different methodological approaches are required.

The evidence-based medicine (EBM) movement was established to combat capricious reasoning in clinical care, particularly arguments from authorities in the field. The critique of authority and appraisal of evidence remain EBM's core values and should be revisited in this era of EBM's maturity and influence. We are now faced with a new form of under-questioned authority and evidence from well-designed and methodologically appraised RCTs. The evidence from RCTs is now prized, even when it is incapable of providing meaningful information, particularly when the underlying causal theory is inscrutable. The evidence obtained from experimental trials in support of remote IP provides us with an illustrative view that highlights systematic scientific blind spots in the institutions of EBM. At its core, medicine, including evidence-based medicine, is based on theory. Thus, EBM must cultivate greater capacity to address the crucial role of theory in both the generation and use of experimental evidence21.

This study was designed, conducted and reported in accordance with the Consolidated Standards of Reporting Trials (CONSORT)22. The most recent guidelines for conducting RCTs were also taken into account23.

Collaborators

FR Silva, MI Rosa, designed the study, drafted the manuscript and analyzed the data. BR Silva, AM Bergamo, LC Costa, R Azevedo and IDE Battisti conceptualized the study, interpreted the data and critically evaluated the manuscript. LR Medeiros, NC Silva and MI Rosa revised and critically evaluated the manuscript.

Acknowledgments

This work was supported by the Foundation for the Support of Scientific and Technological Research of Santa Catarina (FAPESC).

Artigo apresentado em 20/06/2012

Aprovado em 17/09/2012

Versão final apresentada em 02/10/2012

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Publication Dates

  • Publication in this collection
    02 Apr 2013
  • Date of issue
    Aug 2013

History

  • Received
    20 June 2012
  • Accepted
    17 Sept 2012
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