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- W2100963896 abstract "The purpose of this study was to explore cancer patients' experiences with the process of consenting to participate in experimental, randomized design studies. A descriptive study using focus groups was conducted to gain a better understanding of how to improve and facilitate consent discussions between investigators and patients. Categories were defined using a deductive approach based on the literature and the Medical Research Council of Canada (MRC) framework for the consent process. The focus group sessions addressed the question of Now that I have been through the clinical trial research process, what would I have liked to have known?. Implications for nursing practice and recommendations for defining the consent process from the participants' perspective are outlined." @default.
- W2100963896 created "2016-06-24" @default.
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- W2100963896 date "1996-01-01" @default.
- W2100963896 modified "2023-09-25" @default.
- W2100963896 title "Consenting to participate in research for the treatment of cancer: The patient's perspective" @default.
- W2100963896 doi "https://doi.org/10.5737/1181912x63124129" @default.
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