Attitudes Toward Risk and Informed Consent for Research on Medical Practices: A Cross-sectional Survey

BACKGROUND: The U.S. Office for Human Research Protections has proposed that end points of randomized trials comparing the effectiveness of standard medical practices are risks of research that would require disclosure and written informed consent, but data are lacking on the views of potential part...

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Detalhes bibliográficos
Publicado no:Ann Intern Med
Main Authors: Cho, Mildred K., Magnus, David, Constantine, Melissa, Lee, Sandra Soo-Jin, Kelley, Maureen, Alessi, Stephanie, Korngiebel, Diane, James, Cyan, Kuwana, Ellen, Gallagher, Thomas H., Diekema, Douglas, Capron, Alexander M., Joffe, Steven, Wilfond, Benjamin S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4776759/
https://ncbi.nlm.nih.gov/pubmed/25868119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7326/M15-0166
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