Angwenyi, V., Kamuya, D., Mwachiro, D., Marsh, V., Njuguna, P., and Molyneux, S. 2013. Working with Community Health Workers as ‘volunteers’ in a vaccine trial: practical and ethical experiences and implications. Developing World Bioethics, 13, 38–47.
Chambers, R. 2008. Revolutions in development inquiry. London: Earthscan.
Cheah, P. Y., Lwin, K. M., Phaiphun, L., et al. 2010. Community engagement on the Thai-
Burmese border: rationale, experience and lessons learnt. International Health, 2, 123–9.Gikonyo, C., Bejon, P., Marsh, V., and Molyneux, S. 2008. Taking social relationships seri-
ously: lessons learned from the informed consent practices of a vaccine trial on the Kenyan
Coast. Social Science & Medicine, 67, 708–20.
Gikonyo, C., Kamuya, D., Mbete, B., et al. 2013. Feedback of research findings for vaccine tri-
als: experiences from two malaria vaccine trials involving healthy children on the Kenyan
Coast. Developing World Bioethics, 13, 48–56.
Kamuya, D. M., Marsh, V., Kombe, F. K., Geissler, P. W., and Molyneux, S. C. 2013. Engaging
communities to strengthen research ethics in low-income settings: selection and percep- tions of members of a network of representatives in coastal Kenya. Developing World Bioeth- ics, 13, 10–20.
Lavery, J. V., Tinadana, P. O., Scott, T. W., et al. 2010. Towards a framework for community engagement in global health research. Trends in Parasitology, 26, 279–83.
Marsh, V. M., Kamuya, D. M., Mlamba, A. M., Williams, T. N., and Molyneux, S. S. 2010. Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya. BMC Medical Ethics, 11, 13.
Marsh, V. M., Kamuya, D. K., Parker, M. J., and Molyneux, C. S. 2011. Working with Con- cepts: The Role of Community in International Collaborative Biomedical Research. Public Health Ethics, 4, 26–39.
Molyneux, S., Kamuya, D., Madiega, P. A., Chantler, T., Angwenyi, V., and Geissler, P. W.
2013. Field workers at the interface. Developing World Bioethics, 13, ii–iv.
Molyneux, S., Mulupi, S., Mbaabu, L., and Marsh, V. 2012. Benefits and payments for research participants: experiences and views from a research centre on the Kenyan coast. BMC Medi-
cal Ethics, 13, 13.
Ndebele, P. M., Wassenaar, D., Munalula, E., and Masiye, F. 2012. Improving understanding
of clinical trial procedures among low literacy populations: an intervention within a micro-
bicide trial in Malawi. BMC Medical Ethics, 13, 29.
Participants in the Community Engagement Consent Workshop. 2013. Consent and com-
munity engagement in diverse research contexts. Journal of Empirical Research on Human
Research Ethics, 8, 1–18.
Reddy, P., Buchanan, D., Sifunda, S., James, S., and Naidoo, N. 2010. The role of community
advisory boards in health research: divergent views in the South African experience. SA-
HARA Journal, 7, 2–8.
Shagi, C., Vallely, A., Kasindi, S., et al.; Microbicides Development Programme. 2008. A
model for community representation and participation in HIV prevention trials among
women who engage in transactional sex in Africa. AIDS Care, 20, 1039–49.
Shubis, K., Juma, O., Sharifu, R., Burgess, B., and Abdulla, S. 2009. Challenges of establishing
a Community Advisory Board (CAB) in a low-income, low-resource setting: experiences from Bagamoyo, Tanzania. Health Research Policy and Systems, 7, 16.