TY - JOUR
T1 - Ethical issues in cluster randomized trials conducted in low- A nd middle-income countries: An analysis of two case studies: An analysis of two case studies
AU - Choko, Augustine
AU - Roshandel, Gholamreza
AU - Conserve, Donaldson F.
AU - Corbett, Elizabeth L.
AU - Fielding, Katherine
AU - Hemming, Karla
AU - Malekzadeh, Reza
AU - Weijer, Charles
PY - 2020/4/16
Y1 - 2020/4/16
N2 - Background: Cluster randomized trials are common in health research in low- A nd middle-income countries raising issues that challenge interpretation of standard ethical guidelines. While the Ottawa Statement on the ethical design and conduct of cluster randomized trials provides guidance for researchers and research ethics committees, it does not explicitly focus on low- A nd middle-income settings. Main body: In this paper, we use the lens of the Ottawa Statement to analyze two cluster randomized trials conducted in low- A nd middle-income settings in order to identify gaps or ethical issues requiring further analysis and guidance. The PolyIran trial was a parallel-arm, cluster trial examining the effectiveness of a polypill for prevention of cardiovascular disease in Golestan province, Iran. The PASTAL trial was an adaptive, multistage, parallel-arm, cluster trial evaluating the effect of incentives for human immunodeficiency virus self-testing and follow-up on male partners of pregnant women in Malawi. Through an in-depth case analysis of these two studies we highlight several issues in need of further exploration. First, standards for verbal consent and waivers of consent require methods for operationalization if they are to be employed consistently. Second, the appropriate choice of a control arm remains contentious. Particularly in the case of implementation interventions, locally available care is required as the comparator to address questions of comparative effectiveness. However, locally available care might be lower than standards set out in national guidelines. Third, while the need for access to effective interventions post-trial is widely recognized, it is often not possible to guarantee this upfront. Clarity on what is required of researchers and sponsors is needed. Fourth, there is a pressing need for ethics education and capacity building regarding cluster randomized trials in these settings. Conclusion: We identify four issues in cluster randomized trials conducted in low- A nd middle-income countries for which further ethical analysis and guidance is required.
AB - Background: Cluster randomized trials are common in health research in low- A nd middle-income countries raising issues that challenge interpretation of standard ethical guidelines. While the Ottawa Statement on the ethical design and conduct of cluster randomized trials provides guidance for researchers and research ethics committees, it does not explicitly focus on low- A nd middle-income settings. Main body: In this paper, we use the lens of the Ottawa Statement to analyze two cluster randomized trials conducted in low- A nd middle-income settings in order to identify gaps or ethical issues requiring further analysis and guidance. The PolyIran trial was a parallel-arm, cluster trial examining the effectiveness of a polypill for prevention of cardiovascular disease in Golestan province, Iran. The PASTAL trial was an adaptive, multistage, parallel-arm, cluster trial evaluating the effect of incentives for human immunodeficiency virus self-testing and follow-up on male partners of pregnant women in Malawi. Through an in-depth case analysis of these two studies we highlight several issues in need of further exploration. First, standards for verbal consent and waivers of consent require methods for operationalization if they are to be employed consistently. Second, the appropriate choice of a control arm remains contentious. Particularly in the case of implementation interventions, locally available care is required as the comparator to address questions of comparative effectiveness. However, locally available care might be lower than standards set out in national guidelines. Third, while the need for access to effective interventions post-trial is widely recognized, it is often not possible to guarantee this upfront. Clarity on what is required of researchers and sponsors is needed. Fourth, there is a pressing need for ethics education and capacity building regarding cluster randomized trials in these settings. Conclusion: We identify four issues in cluster randomized trials conducted in low- A nd middle-income countries for which further ethical analysis and guidance is required.
KW - Cluster randomized trial
KW - Equipoise
KW - Ethics
KW - Informed consent
KW - Low- A nd middle-income countries
KW - Post-trial access
KW - Research ethics
KW - Research ethics committee
U2 - 10.1186/s13063-020-04269-3
DO - 10.1186/s13063-020-04269-3
M3 - Article
SN - 1745-6215
VL - 21
JO - Trials
JF - Trials
M1 - 314
ER -