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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...
Autor principal: | Kaye, Dan Kabonge |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
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 |
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