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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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Bibliografische gegevens
Gepubliceerd in:Clin Trials
Hoofdauteurs: Kass, Nancy, Taylor, Holly, Ali, Joseph, Hallez, Kristina, Chaisson, Lelia
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2014
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Online toegang: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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