Department of Quantitative Health Sciences
Medical Subject Headings
Cluster Analysis; Epidemiologic Research Design; Humans; Randomized Controlled Trials as Topic
Bioethics and Medical Ethics | Epidemiology | Health Services Research
- In cluster randomized trials (CRTs), the units of allocation, intervention, and outcome measurement may differ within a single trial. As a result of the unique design of CRTs, the interpretation of existing research ethics guidelines is complicated.
- The Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials aims to provide researchers and research ethics committees (RECs) with detailed guidance on the ethical design, conduct, and review of CRTs.
- A five-year mixed methods research project explored the ethical challenges of CRTs. Empirical studies documented the reporting of ethical issues in published CRTs, interviewed experienced trialists, and surveyed trialists and REC chairs. The ethical issues identified were explored in a series of background papers that provided detailed ethical analyses and policy options, and a panel of experts using a systematic process developed a consensus statement.
- The Ottawa Statement sets out 15 recommendations for the ethical design and conduct of CRTs. The recommendations provide guidance on the justification of a cluster randomized design, the need for REC review, the identification of research participants, obtaining informed consent, the role of gatekeepers in protecting group interests, the assessment of benefits and harms, and the protection of vulnerable participants.
Weijer, Charles; Grimshaw, Jeremy M.; Eccles, Martin P.; McRae, Andrew D.; White, Angela; Brehaut, Jamie C.; Taljaard, Monica; Ottawa Ethics of Cluster Randomized Trials Consensus Group; and Kiefe, Catarina I., "The Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials" (2012). Quantitative Health Sciences Publications and Presentations. 1107.