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Communicating the Results of Clinical Research to Participants: Attitudes, Practices, and Future Directions

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  • David I Shalowitz
  • Franklin G Miller

Abstract

The authors discuss the available data on the effects of communicating aggregate and individual research results on participants, investigators, and the research enterprise.

Suggested Citation

  • David I Shalowitz & Franklin G Miller, 2008. "Communicating the Results of Clinical Research to Participants: Attitudes, Practices, and Future Directions," PLOS Medicine, Public Library of Science, vol. 5(5), pages 1-7, May.
    • Handle: RePEc:plo:pmed00:0050091
    DOI: 10.1371/journal.pmed.0050091
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    References listed on IDEAS

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    1. Theresa M. Marteau & Scott Roberts & Susan LaRusse & Robert C. Green, 2005. "Predictive Genetic Testing for Alzheimer's Disease: Impact upon Risk Perception," Risk Analysis, John Wiley & Sons, vol. 25(2), pages 397-404, April.
    2. Bayer, R., 1986. "Notifying workers at risk: The politics of the right-to-know," American Journal of Public Health, American Public Health Association, vol. 76(11), pages 1352-1356.
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