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Consent Timing and Experience: Modifiable Factors That May Influence Interest in Clinical Research

PURPOSE: Low rates of participation in cancer clinical trials have been attributed to patient, institutional, and study characteristics. However, few studies have examined factors related to the consent process. We therefore evaluated the impact of consent timing and experience on markers of patient...

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Detalhes bibliográficos
Main Authors: Gerber, David E., Rasco, Drew W., Skinner, Celette Sugg, Dowell, Jonathan E., Yan, Jingsheng, Sayne, Jennifer R., Xie, Yang
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Clinical Oncology 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3457835/
https://ncbi.nlm.nih.gov/pubmed/23077435
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1200/JOP.2011.000335
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