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Research with Decisionally Incapacitated Human Subjects: An Argument for a Systemic Approach to Risk-Benefit Assessment


Carl H. Coleman


Seton Hall University School of Law


Indiana Law Journal, Forthcoming
Seton Hall Public Law Research Paper No. 979704

Abstract:     
The amount of medical research with persons who lack decision-making capacity is rapidly increasing, but in most states it takes place without clear legal authority. In addition to creating significant liability risks for researchers and persons who provide consent on behalf of incapacitated subjects, the lack of explicit legal standards means that few, if any, safeguards exist to protect incapacitated persons' rights and welfare. Previous efforts to close the gap between clinical reality and legal requirements have failed in part because they have not provided a coherent or persuasive ethical justification for permitting this research. This Article seeks to fill that void by proposing a new way of thinking about the ethics of research with incapacitated persons, grounded in a long-term, systemic approach to risk-benefit assessment. This approach explains why it is ultimately in incapacitated persons' best interests to be governed by a policy that permits them to be enrolled in research without their personal authorization¿even if such a policy puts them at risk of participating in studies that, when viewed in isolation, may involve more burdens than benefits. Unlike other approaches, the framework developed here does not depend on false analogies between participating in research and receiving medical treatment, or dubious claims about family members' inherent authority or incapacitated persons' obligations to society. Because the proposed framework directly responds to the criticism that research with incapacitated persons is a form of exploitation, it may increase the likelihood that proposals to authorize this research will actually be adopted. It also has important implications for both how laws governing research with incapacitated persons should be structured, and the roles and responsibilities of surrogate decision makers.

Number of Pages in PDF File: 47

Keywords: medical research, human subjects, incapacity, surrogate consent

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Date posted: April 13, 2007 ; Last revised: February 14, 2014

Suggested Citation

Coleman, Carl H., Research with Decisionally Incapacitated Human Subjects: An Argument for a Systemic Approach to Risk-Benefit Assessment. Indiana Law Journal, Forthcoming; Seton Hall Public Law Research Paper No. 979704. Available at SSRN: http://ssrn.com/abstract=979704

Contact Information

Carl H. Coleman (Contact Author)
Seton Hall University School of Law ( email )
One Newark Center
Newark, NJ 07102-5210
United States
201-204-9512 (Phone)
973-642-8194 (Fax)
HOME PAGE: http://law.shu.edu/Faculty/fulltime_faculty/Carl-Coleman.cfm
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