Researchers experience and views on participants’ comprehension of informed consent in clinical trials in Malawi: a descriptive qualitative study
Most of the participants understand much of the information during subsequent visits as you keep reminding them since informed consent is an ongoing process. Existing relationship or trust between a participant and a researcher, may influence participants' decision and misguide their understanding on the purpose of the study. Adequate time should be allocated to informed consent discussions. Shortening the informed consent forms and having additional conversations with potential participants may help improve their understanding.
Authors
- Dorothy Kazembe
- Solomón Mequanente Abay (ORCID: https://orcid.org/0000-0002-7844-3771)
- Yimtubezinash Woldeamanuel
Institutions
- University of Liverpool (GB)
- Malawi-Liverpool-Wellcome Trust Clinical Research Programme (MW)
- Africa Centres for Disease Control and Prevention (ET)
- Addis Ababa University (ET)
Publication Details
- Journal
- BMC Medical Ethics
- Published
- 2024-09-27
- DOI
- https://doi.org/10.1186/s12910-024-01100-5
- Citations
- 1
- Primary Topic
- Ethics in Clinical Research
- Type
- article
- Field-Weighted Citation Impact
- 0.54
Funders
- Addis Ababa University