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A Digital Health App to Assess Decisional Capacity to Provide Informed Consent: Protocol for a Randomized Controlled Trial

BACKGROUND: Any study with human subjects must have a robust consent process to ensure that participants understand the study and can decide whether they want to be involved. Investigators must determine whether a potential study participant is able to make an informed decision and what modification...

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Detalles Bibliográficos
Autores principales:	Furberg, Robert D, Raspa, Melissa, Wheeler, Anne C, McCormack, Lauren A, Bailey, Donald B
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	JMIR Publications 2018
Materias:	Protocol
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277828/ https://www.ncbi.nlm.nih.gov/pubmed/30455171 http://dx.doi.org/10.2196/10360

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