Volunteer human subjects' understandings of their participation in a biomedical research experiment
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- Snowdon, Claire & Garcia, Jo & Elbourne, Diana, 1997. "Making sense of randomization; responses of parents of critically ill babies to random allocation of treatment in a clinical trial," Social Science & Medicine, Elsevier, vol. 45(9), pages 1337-1355, November.
- Lidz, Charles W. & Appelbaum, Paul S. & Grisso, Thomas & Renaud, Michelle, 2004. "Therapeutic misconception and the appreciation of risks in clinical trials," Social Science & Medicine, Elsevier, vol. 58(9), pages 1689-1697, May.
- Featherstone, Katie & Donovan, Jenny L., 2002. ""Why don't they just tell me straight, why allocate it?" The struggle to make sense of participating in a randomised controlled trial," Social Science & Medicine, Elsevier, vol. 55(5), pages 709-719, September.
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Cited by:
- Dixon-Woods, Mary & Ashcroft, Richard E. & Jackson, Clare J. & Tobin, Martin D. & Kivits, Joelle & Burton, Paul R. & Samani, Nilesh J., 2007. "Beyond "misunderstanding": Written information and decisions about taking part in a genetic epidemiology study," Social Science & Medicine, Elsevier, vol. 65(11), pages 2212-2222, December.
- Mein, Gill & Seale, Clive & Rice, Helen & Johal, Suneeta & Ashcroft, Richard E. & Ellison, George & Tinker, Anthea, 2012. "Altruism and participation in longitudinal health research? Insights from the Whitehall II Study," Social Science & Medicine, Elsevier, vol. 75(12), pages 2345-2352.
- Elberse, Janneke Elisabeth & Pittens, Carina Anna Cornelia Maria & de Cock Buning, Tjard & Broerse, Jacqueline Elisabeth Willy, 2012. "Patient involvement in a scientific advisory process: Setting the research agenda for medical products," Health Policy, Elsevier, vol. 107(2), pages 231-242.
- Fisher, Jill A., 2008. "Practicing research ethics: Private-sector physicians & pharmaceutical clinical trials," Social Science & Medicine, Elsevier, vol. 66(12), pages 2495-2505, June.
- Fisher, Jill A. & Cottingham, Marci D. & Kalbaugh, Corey A., 2015. "Peering into the pharmaceutical “pipeline”: Investigational drugs, clinical trials, and industry priorities," Social Science & Medicine, Elsevier, vol. 131(C), pages 322-330.
- Cox, Susan M. & McDonald, Michael, 2013. "Ethics is for human subjects too: Participant perspectives on responsibility in health research," Social Science & Medicine, Elsevier, vol. 98(C), pages 224-231.
- Murphy, Elizabeth & Dingwall, Robert, 2007. "Informed consent, anticipatory regulation and ethnographic practice," Social Science & Medicine, Elsevier, vol. 65(11), pages 2223-2234, December.
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Keywords
UK Human research subjects Volunteers Researcher-subject relationship Patient participation Human experimentation;Statistics
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