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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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Publicado en:Clin Trials
Main Authors: Kass, Nancy, Taylor, Holly, Ali, Joseph, Hallez, Kristina, Chaisson, Lelia
Formato: Artigo
Idioma:Inglês
Publicado: 2014
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Acceso en liña: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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