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Participant Informed Consent in Cluster Randomized Trials: Review

BACKGROUND: The Nuremberg code defines the general ethical framework of medical research with participant consent as its cornerstone. In cluster randomized trials (CRT), obtaining participant informed consent raises logistic and methodologic concerns. First, with randomization of large clusters such...

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Autors principals: Giraudeau, Bruno, Caille, Agnès, Le Gouge, Amélie, Ravaud, Philippe
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2012
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3391275/
https://ncbi.nlm.nih.gov/pubmed/22792319
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0040436
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