Abstract

BackgroundCluster randomized trials (CRTs) present unique ethical challenges. In the absence of a uniform standard for their ethical design and conduct, problems such as variability in procedures and requirements by different research ethics committees will persist. We aimed to assess the need for ethics guidelines for CRTs among research ethics chairs internationally, investigate variability in procedures for research ethics review of CRTs within and among countries, and elicit research ethics chairs’ perspectives on specific ethical issues in CRTs, including the identification of research subjects. The proper identification of research subjects is a necessary requirement in the research ethics review process, to help ensure, on the one hand, that subjects are protected from harm and exploitation, and on the other, that reviews of CRTs are completed efficiently.MethodsA web-based survey with closed- and open-ended questions was administered to research ethics chairs in Canada, the United States, and the United Kingdom. The survey presented three scenarios of CRTs involving cluster-level, professional-level, and individual-level interventions. For each scenario, a series of questions was posed with respect to the type of review required (full, expedited, or no review) and the identification of research subjects at cluster and individual levels.ResultsA total of 189 (35%) of 542 chairs responded. Overall, 144 (84%, 95% CI 79 to 90%) agreed or strongly agreed that there is a need for ethics guidelines for CRTs and 158 (92%, 95% CI 88 to 96%) agreed or strongly agreed that research ethics committees could be better informed about distinct ethical issues surrounding CRTs. There was considerable variability among research ethics chairs with respect to the type of review required, as well as the identification of research subjects. The cluster-cluster and professional-cluster scenarios produced the most disagreement.ConclusionsResearch ethics committees identified a clear need for ethics guidelines for CRTs and education about distinct ethical issues in CRTs. There is disagreement among committees, even within the same countries, with respect to key questions in the ethics review of CRTs. This disagreement reflects variability of opinion and practices pointing toward possible gaps in knowledge, and supports the need for explicit guidelines for the ethical conduct and review of CRTs.

Highlights

  • Cluster randomized trials (CRTs) present unique ethical challenges

  • It is convenient to distinguish between three kinds of CRTs depending on the level of intervention: cluster-cluster trials, professional-cluster trials, and individual-cluster trials [3,4]

  • In the Nexus trial, an example of a professional-cluster trial, 247 primary care practices were randomized to evaluate the effect of audit and feedback and reminder messages on radiology referrals [6], while in the bed net trial, an example of an individual-cluster trial, 36 villages were randomized to evaluate the impact of distribution of insecticide-treated bed nets to individual citizens on malaria morbidity and mortality in remote areas of Cambodia [7]

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Summary

Introduction

Cluster randomized trials (CRTs) present unique ethical challenges. In the absence of a uniform standard for their ethical design and conduct, problems such as variability in procedures and requirements by different research ethics committees will persist. In the absence of guidance tailored to CRTs, researchers and research ethics committees have had to rely on variable interpretation of existing research ethics guidelines, which were developed primarily with individually randomized trials in mind. This has likely contributed to variation in how CRTs have been conducted in practice, as well as in the requirements and decisions by different research ethics committees [11,12]. As part of the effort to develop these guidelines, we conducted a web-based survey of chairs of research ethics committees (Research Ethics Boards (REBs) in Canada, Research Ethics Committees (RECs) in the United Kingdom, Institutional Review Boards (IRBs) in the United States). The main objectives of this survey were to a) evaluate the need among research ethics committees for guidelines specific to CRTs, b) gather information about the research ethics review process for CRTs at their institutions, and c) elicit their views on ethical issues in CRTs using a scenario-based approach

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