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Protection of Human Subjects

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Encyclopedia of Behavioral Medicine
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Human subjects protections

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The organized oversight of research to ensure the rights and well-being of participants.

Description

The protection of human subjects in clinical research evolved in response to conditions surrounding medical research that were deemed unacceptable in the early to mid-twentieth century. In December 1946, an American military tribunal opened criminal proceedings against 23 German physicians who conducted medical experiments on thousands of concentration camp prisoners without their consent. Most of the subjects of these experiments died or were permanently disabled as a result. The Nuremberg Code of 1948 resulted, stating that “voluntary consent of a human subject is absolutely essential” and that “the benefits of research must outweigh the risks” (NIH). In 1964, the World Medical Association published recommendations for research involving human subjects, and the Declaration of Helsinki governs international research ethics and defines...

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Correspondence to Marianne Shaughnessy .

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© 2013 Springer Science+Business Media, New York

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Shaughnessy, M. (2013). Protection of Human Subjects. In: Gellman, M.D., Turner, J.R. (eds) Encyclopedia of Behavioral Medicine. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-1005-9_1573

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  • DOI: https://doi.org/10.1007/978-1-4419-1005-9_1573

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4419-1004-2

  • Online ISBN: 978-1-4419-1005-9

  • eBook Packages: MedicineReference Module Medicine

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