Complex and alternate consent pathways in clinical trials: methodological and ethical challenges encountered by underserved groups and a call to action

Abstract Background Informed consent is considered a fundamental requirement for participation in trials, yet obtaining consent is challenging in a number of populations and settings. This may be due to participants having communication or other disabilities, their capacity to consent fluctuates or...

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Detalhes bibliográficos

Principais autores:	Amy M. Russell, Victoria Shepherd, Kerry Woolfall, Bridget Young, Katie Gillies, Anna Volkmer, Mark Jayes, Richard Huxtable, Alexander Perkins, Nurulamin M. Noor, Beverley Nickolls, Julia Wade
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMC 2023-02-01
Colecção:	Trials
Assuntos:	Informed consent Clinical trials Ethics Underserved populations
Acesso em linha:	https://doi.org/10.1186/s13063-023-07159-6
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