The impact of central IRB's on informed consent readability and trial adherence in SPRINT

BACKGROUND: Federal agencies have encouraged the use of central institutional review boards (CIRBs) for multi-site clinical trials. There is limited evidence supporting the use of CIRBs. Our aim is to evaluate how SPRINT sites regulated by CIRBs performed regarding informed consent readability and p...

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Detalhes bibliográficos
Publicado no:Contemp Clin Trials Commun
Main Authors: Tamariz, Leonardo, Gajardo, Mitscher, Still, Carolyn H., Gren, Lisa H., Clark, Elizabeth, Walsh, Sandy, Whittle, Jeff, Nord, John, Ramsey, Thomas, Contreras, Gabriel
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6627564/
https://ncbi.nlm.nih.gov/pubmed/31338481
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.conctc.2019.100407
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