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...
Main Authors: | Leonardo Tamariz, Mitscher Gajardo, Carolyn H. Still, Lisa H. Gren, Elizabeth Clark, Sandy Walsh, Jeff Whittle, John Nord, Thomas Ramsey, Gabriel Contreras |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2019-09-01
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Series: | Contemporary Clinical Trials Communications |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2451865418302023 |
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