Motivation to participate and experiences of the informed consent process for randomized clinical trials in emergency obstetric care in Uganda

BACKGROUND: Informed consent, whose goal is to assure that participants enter research voluntarily after disclosure of potential risks and benefits, may be impossible or impractical in emergency research. In low resource settings, there is limited information on the experiences of the informed conse...

Descripción completa

Detalles Bibliográficos
Autor principal: Kaye, Dan Kabonge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317416/
https://www.ncbi.nlm.nih.gov/pubmed/34320963
http://dx.doi.org/10.1186/s12910-021-00672-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317416/
https://www.ncbi.nlm.nih.gov/pubmed/34320963
http://dx.doi.org/10.1186/s12910-021-00672-w

Ejemplares similares