Development of a decision support intervention for family members of adults who lack capacity to consent to trials

BACKGROUND: Informed consent is required for participation in clinical trials, however trials involving adults who lack capacity to consent require different enrolment processes. A family member usually acts as a proxy to make a decision based on the patient’s ‘presumed will’, but these decisions ca...

Descripción completa

Detalles Bibliográficos
Autores principales: Shepherd, Victoria, Wood, Fiona, Griffith, Richard, Sheehan, Mark, Hood, Kerenza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Technical Advance
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842028/
https://www.ncbi.nlm.nih.gov/pubmed/33509169
http://dx.doi.org/10.1186/s12911-021-01390-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842028/
https://www.ncbi.nlm.nih.gov/pubmed/33509169
http://dx.doi.org/10.1186/s12911-021-01390-4

Ejemplares similares