Community engagement approaches and lessons learned: a case study of the PRECISE pregnancy cohort study in Kenya
Community engagement (CE) has been recommended as an important ethical consideration for health research to enhance informed consent and exchange knowledge between researchers and community members. The purpose of this paper is to describe how CE was developed and delivered for the PRECISE prospective pregnancy cohort study in Kenya. PRECISE enrolled pregnant women in antenatal care, followed them up to the postpartum period, and collected data and biological samples to enable the study of placental disorders in sub-Saharan Africa. Initially CE was aimed at informing the community about the study, establishing community-wide acceptance of the research and addressing concerns about biological sample collection to facilitate participation in the study. CE later evolved to be a platform for mutual learning aiming to deepen the community's understanding of research principles and informed consent and providing a feedback loop to researchers. We engaged diverse stakeholders including health workers and managers, local administrators, religious and traditional leaders, older women, pregnant women, non-pregnant women and men. We utilized a variety of CE approaches and tools adapting to the specific contextual factors at the study sites. Achievements included widespread understanding of informed consent and research principles, clarification of misconceptions, and dispelling of fears regarding biological sample collection. The relationship with the community was strengthened evidenced by frequent inquiries and active participation in CE activities and the research study. For effective CE, we recommend involvement of community members in the CE team and continuous and adaptive CE throughout the study period.
Authors
- Marie‐Laure Volvert (ORCID: https://orcid.org/0000-0002-0527-4145)
- Grace Mkanjala Mwashigadi (ORCID: https://orcid.org/0000-0002-6321-3287)
- Hiten D. Mistry (ORCID: https://orcid.org/0000-0003-2564-7348)
- Marianne Vidler (ORCID: https://orcid.org/0000-0002-7633-8812)
- Angela C. Koech (ORCID: https://orcid.org/0000-0003-4838-3269)
- Mai‐Lei Woo Kinshella (ORCID: https://orcid.org/0000-0001-5846-3014)
- Alice Kombo
- Peter von Dadelszen (ORCID: https://orcid.org/0000-0003-4136-3070)
- Marleen Temmerman (ORCID: https://orcid.org/0000-0001-9966-9000)
- Onesmus Wanje (ORCID: https://orcid.org/0000-0002-0271-2533)
- Nathan Barreh
- Rachel Craik
- Grace Maitha
Institutions
- University of British Columbia (CA)
- University of Leicester (GB)
- King's College London (GB)
- Ghent University (BE)
- Aga Khan University Nairobi (KE)
Publication Details
- Journal
- Frontiers in Public Health
- Published
- 2025-03-11
- DOI
- https://doi.org/10.3389/fpubh.2025.1439150
- Citations
- 1
- Primary Topic
- Ethics in Clinical Research
- Type
- article
- Field-Weighted Citation Impact
- 1.88
Funders
- UK Research and Innovation
- National Institutes of Health
- Office of the Director
- National Institute of Mental Health
- Fogarty International Center
- National Institute of Biomedical Imaging and Bioengineering