PMID: 11323128Apr 27, 2001Paper

Obtaining informed consent for clinical pain research: patients' concerns and information needs

Pain
David CasarettDavid A Asch

Abstract

Investigators who conduct clinical pain research are required to obtain voluntary informed consent from patients. However, little is known about what information patients expect when they decide whether to enroll in such studies. It is important that investigators understand these information needs so they can effectively and clearly describe the research risks and potential benefits that matter to potential subjects. By understanding these needs for information, investigators may also be better able to anticipate patients' concerns and to recruit subjects more efficiently. This study was designed to define information needs that patients have when they decide whether to participate in clinical pain research. This paper describes these information needs, and identifies clinical and demographic variables associated with specific needs.

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Citations

Aug 2, 2007·Journal of General Internal Medicine·Jacquelyn SlomkaMark L Williams
Dec 10, 2002·Neurobiology of Aging·Jason H T Karlawish, Christopher M Clark
Jan 19, 2002·Journal of Palliative Medicine·D CasarettP Silverman
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Jan 19, 2010·Research in Gerontological Nursing·Melissa Lehan MackinSara Sanders
Apr 13, 2013·European Journal of Pain : EJP·D Loreto-QuijadaR Nieto
Sep 17, 2018·BMC Medical Ethics·Juntra KarbwangUNKNOWN FERCAP Multi-Country Research Team

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