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dc.contributor.authorWeijer, Charles
dc.contributor.authorGrimshaw, Jeremy M.
dc.contributor.authorEccles, Martin P.
dc.contributor.authorMcRae, Andrew D.
dc.contributor.authorWhite, Angela
dc.contributor.authorBrehaut, Jamie C.
dc.contributor.authorTaljaard, Monica
dc.contributor.authorOttawa Ethics of Cluster Randomized Trials Consensus Group
dc.contributor.authorKiefe, Catarina I.
dc.date2022-08-11T08:10:34.000
dc.date.accessioned2022-08-23T17:13:05Z
dc.date.available2022-08-23T17:13:05Z
dc.date.issued2012-11-12
dc.date.submitted2013-04-29
dc.identifier.citationWeijer C, Grimshaw JM, Eccles MP, McRae AD, White A, et al. (2012) The Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials. PLoS Med 9(11): e1001346. doi:10.1371/journal.pmed.1001346. <a href="http://dx.doi.org/10.1371/journal.pmed.1001346" target="_blank">Link to article on publisher's website</a>
dc.identifier.issn1549-1676
dc.identifier.doi10.1371/journal.pmed.1001346
dc.identifier.pmid23185138
dc.identifier.urihttp://hdl.handle.net/20.500.14038/46647
dc.description<p>Catarina Kiefe is a member of the Ottawa Ethics of Cluster Randomized Trials Consensus Group.</p>
dc.description.abstractSummary points: 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.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=23185138&dopt=Abstract">Link to article in PubMed</a>
dc.rights<p>Copyright 2012 Weijer et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</p>
dc.subjectCluster Analysis
dc.subjectEpidemiologic Research Design
dc.subjectHumans
dc.subjectRandomized Controlled Trials as Topic
dc.subjectUMCCTS funding
dc.subjectBioethics and Medical Ethics
dc.subjectEpidemiology
dc.subjectHealth Services Research
dc.titleThe Ottawa Statement on the Ethical Design and Conduct of Cluster Randomized Trials
dc.typeJournal Article
dc.source.journaltitlePLoS medicine / Public Library of Science
dc.source.volume9
dc.source.issue11
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2107&amp;context=qhs_pp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/qhs_pp/1107
dc.identifier.contextkey4082453
refterms.dateFOA2022-08-23T17:13:05Z
html.description.abstract<p>Summary points: <ul> <li>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.</li> <li>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.</li> <li>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.</li> <li>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.</li> </ul></p>
dc.identifier.submissionpathqhs_pp/1107
dc.contributor.departmentDepartment of Quantitative Health Sciences
dc.source.pagese1001346


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