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  1. Protecting communities in health research from exploitation.Segun Gbadegesin & David Wendler - 2006 - Bioethics 20 (5):248-253.
    Guidelines for health research focus on protecting individual research subjects. It is also vital to protect the communities involved in health research. In particular, a number of studies have been criticized on the grounds that they exploited host communities. The present paper attempts to address these concerns by providing an analysis of community exploitation and, based on this analysis, determining what safeguards are needed to protect communities in health research against exploitation. (edited).
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  • Understanding of Research: a Sri Lankan Perspective.Athula Sumathipala, Sisira Siribaddana, Suwin Hewage, Manura Lekamwattage, Manjula Athukorale, Chesmal Siriwardhana, Kumudu Munasinghe, Kethakie Sumathipala, Joanna Murray & Martin Prince - 2010 - BMC Medical Ethics 11 (1):7-.
    BackgroundLack of proper understanding on the part of researchers about public understanding of research and informed consent will increase the potential for malpractice. As a part of a larger study on ethics and informed consent in Sri Lanka, this study aimed to ascertain the level of understanding of 'research' by exploring the views of the public and professionals.MethodsConvenience sampling and snow ball technique were used for recruitment with an emphasis on balanced age and gender representation, diverse educational, socio-cultural and professional (...)
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  • Community based trials and informed consent in rural north India.A. DeCosta - 2004 - Journal of Medical Ethics 30 (3):318-323.
    Disease control has increasingly shifted towards large scale, disease specific, public health interventions. The emerging problems of HIV, hepatitis, malaria, typhoid, tuberculosis, childhood pneumonia, and meningitis have made community based trials of interventions a cost effective long term investment for the health of a population. The authors conducted this study to explore the complexities involved in obtaining informed consent to participation in rural north India, and how people there make decisions related to participation in clinical research.
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