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...

Descripción completa

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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277828/
https://www.ncbi.nlm.nih.gov/pubmed/30455171
http://dx.doi.org/10.2196/10360

Ejemplares similares