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A Pilot Study of Simple Interventions to Improve Informed Consent in Clinical Research: Feasibility, Approach, and Results

BACKGROUND: Informed consent is intended to ensure that individuals understand the purpose, risks, and benefits of research studies, and then can decide, voluntarily, whether to enroll. However, research suggests that consent procedures do not always lead to adequate participant understanding and ma...

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Detalhes bibliográficos
Publicado no:Clin Trials
Main Authors: Kass, Nancy, Taylor, Holly, Ali, Joseph, Hallez, Kristina, Chaisson, Lelia
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4344898/
https://ncbi.nlm.nih.gov/pubmed/25475879
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1740774514560831
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