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INFORMED CONSENT IN CLINICAL TRIALS FOR PERSONS WITH DEMENTIA

Informed consent is one of the most important processes during the implementation of a clinical trial; special attention must be given to meeting the needs of persons with dementia in nursing homes who have impaired decision making capacity. We overcame several challenges during enrollment and conse...

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Detalles Bibliográficos
Autor principal: Carpenter, Joan G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6840185/
http://dx.doi.org/10.1093/geroni/igz038.106