| Literature DB >> 11558694 |
Abstract
Protecting the rights of research participants when conducting studies within an international context presents many challenges. The purpose of this article was to compare and contrast the process of obtaining informed consent in two very different countries - Swaziland and Pakistan. Major aspects of the informed-consent process presented included identification of gatekeepers, seeking permission from officials, negotiating with these officials and Institutional Review Board (IRB) committees in regard to the type of data to be collected, and explaining informed consent to participants in the field. Data for this article is based upon qualitative research of collaboration between nurses and healers in Swaziland and from a variety of studies completed in Pakistan. These studies demonstrate the inadequacy and complexity of applying western-based concepts of informed consent to developing countries.Entities:
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Year: 2001 PMID: 11558694 DOI: 10.1046/j.1466-7657.2001.00063.x
Source DB: PubMed Journal: Int Nurs Rev ISSN: 0020-8132 Impact factor: 2.871