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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Contemp Clin Trials Commun
Päätekijät: Tamariz, Leonardo, Gajardo, Mitscher, Still, Carolyn H., Gren, Lisa H., Clark, Elizabeth, Walsh, Sandy, Whittle, Jeff, Nord, John, Ramsey, Thomas, Contreras, Gabriel
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2019
Aiheet:
Article
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia