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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Detalles Bibliográficos
Autores principales: Giraudeau, Bruno, Caille, Agnès, Le Gouge, Amélie, Ravaud, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391275/
https://www.ncbi.nlm.nih.gov/pubmed/22792319
http://dx.doi.org/10.1371/journal.pone.0040436

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3391275/
https://www.ncbi.nlm.nih.gov/pubmed/22792319
http://dx.doi.org/10.1371/journal.pone.0040436

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