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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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Bibliographische Detailangaben
Veröffentlicht in:BMC Med Ethics
1. Verfasser: Kaye, Dan Kabonge
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2021
Schlagworte:
Online Zugang: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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