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  1. Lay persons’ perception of the requirements for research in emergency obstetric and newborn care.Dan Kabonge Kaye - 2021 - BMC Medical Ethics 22 (1):1-13.
    Background Factors that could potentially act as facilitators and barriers to successful recruitment strategies in perinatal clinical trials are not well documented. The objective was to assess lay persons’ understanding of the informed consent for randomized clinical trial in emergency obstetric and newborn care. Methods This was a qualitative study conducted among survivors of severe obstetric complications who were attending the post-natal clinic of Kawempe National Referral Hospital, Uganda, 6–8 weeks after surviving severe obstetric complications during pregnancy or childbirth. The (...)
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  • Motivation to participate and experiences of the informed consent process for randomized clinical trials in emergency obstetric care in Uganda.Dan Kabonge Kaye - 2021 - BMC Medical Ethics 22 (1):1-12.
    BackgroundInformed 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 consent process for randomized clinical trials in the emergency care context. The objective of this study was to explore the experiences of the informed consent process and factors that motivated participation in two obstetrics and newborn care randomized clinical trials (...)
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