When is informed consent required in cluster randomized trials in health research?

When is informed consent required in cluster randomized trials in health research?

This article is part of a series of papers examining ethical issues in cluster randomized trials (CRTs) in health research. In the introductory paper in this series, we set out six areas of inquiry that must be addressed if the cluster trial is to be set on a firm ethical foundation. This paper addr...

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Bibliographic Details
Main Authors: McRae, Andrew D, Weijer, Charles, Binik, Ariella, Grimshaw, Jeremy M, Boruch, Robert, Brehaut, Jamie C, Donner, Allan, Eccles, Martin P, Saginur, Raphael, White, Angela, Taljaard, Monica
Format: Online
Language:English
Published: BioMed Central 2011
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184061/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184061/

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