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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Detalles Bibliográficos
Autores principales: Tamariz, Leonardo, Gajardo, Mitscher, Still, Carolyn H., Gren, Lisa H., Clark, Elizabeth, Walsh, Sandy, Whittle, Jeff, Nord, John, Ramsey, Thomas, Contreras, Gabriel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627564/
https://www.ncbi.nlm.nih.gov/pubmed/31338481
http://dx.doi.org/10.1016/j.conctc.2019.100407

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627564/
https://www.ncbi.nlm.nih.gov/pubmed/31338481
http://dx.doi.org/10.1016/j.conctc.2019.100407

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