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  1. Protecting Research Subjects after Consent: The Case for the "Research Intermediary".Stanley Joel Reiser & Paula Knudson - 1993 - IRB: Ethics & Human Research 15 (2):10.
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  • Declaration of Helsinki. Ethical Principles for Medical Research Involving Human Subjects.World Medical Association - 2009 - Jahrbuch für Wissenschaft Und Ethik 14 (1):233-238.
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  • Neuropsychological functioning and recall of research consent information among drug court clients.David S. Festinger, Kattiya Ratanadilok, Douglas B. Marlowe, Karen L. Dugosh, Nicholas S. Patapis & David S. DeMatteo - 2007 - Ethics and Behavior 17 (2):163 – 186.
    Evidence suggests that research participants often fail to recall much of the information provided during the informed consent process. This study was conducted to determine the proportion of consent information recalled by drug court participants following a structured informed consent procedure and the neuropsychological factors that were related to recall. Eighty-five participants completed a standard informed consent procedure to participate in an ongoing research study, followed by a 17-item consent quiz and a brief neuropsychological battery 2 weeks later. Participants performed (...)
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  • The Ethics of Involving Psychiatrically Impaired Persons in Research.Evan Gaines DeRenzo - 1994 - IRB: Ethics & Human Research 16 (6):7.
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