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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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Dades bibliogràfiques
Publicat a:Ann Intern Med
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: 2015
Matèries:
Accés en línia: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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