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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...

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Detalhes bibliográficos
Publicado no:BMC Med Ethics
Autor principal: Kaye, Dan Kabonge
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8317416/
https://ncbi.nlm.nih.gov/pubmed/34320963
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12910-021-00672-w
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