14 found
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  1.  55
    Reframing Consent for Clinical Research: A Function-Based Approach.Scott Y. H. Kim, David Wendler, Kevin P. Weinfurt, Robert Silbergleit, Rebecca D. Pentz, Franklin G. Miller, Bernard Lo, Steven Joffe, Christine Grady, Sara F. Goldkind, Nir Eyal & Neal W. Dickert - 2017 - American Journal of Bioethics 17 (12):3-11.
    Although informed consent is important in clinical research, questions persist regarding when it is necessary, what it requires, and how it should be obtained. The standard view in research ethics is that the function of informed consent is to respect individual autonomy. However, consent processes are multidimensional and serve other ethical functions as well. These functions deserve particular attention when barriers to consent exist. We argue that consent serves seven ethically important and conceptually distinct functions. The first four functions pertain (...)
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  2.  5
    Partnering With Patients to Bridge Gaps in Consent for Acute Care Research.Neal W. Dickert, Amanda Michelle Bernard, JoAnne M. Brabson, Rodney J. Hunter, Regina McLemore, Andrea R. Mitchell, Stephen Palmer, Barbara Reed, Michele Riedford, Raymond T. Simpson, Candace D. Speight, Tracie Steadman & Rebecca D. Pentz - 2020 - American Journal of Bioethics 20 (5):7-17.
    Clinical trials for acute conditions such as myocardial infarction and stroke pose challenges related to informed consent due to time limitations, stress, and severe illness. Consent processes shou...
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  3.  5
    Reframing Recruitment: Evaluating Framing in Authorization for Research Contact Programs.Candace D. Speight, Charlie Gregor, Yi-An Ko, Stephanie A. Kraft, Andrea R. Mitchell, Nyiramugisha K. Niyibizi, Bradley G. Phillips, Kathryn M. Porter, Seema K. Shah, Jeremy Sugarman, Benjamin S. Wilfond & Neal W. Dickert - 2021 - AJOB Empirical Bioethics 12 (3):206-213.
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  4.  2
    When Does Nudging Represent Fraudulent Disclosure?Jennifer Blumenthal-Barby, Neal W. Dickert & Derek Soled - 2021 - American Journal of Bioethics 21 (5):63-66.
    In the article “Informed Consent: What Must be Disclosed and What Must be Understood?” Joseph Millum and Danielle Bromwich argue that informed consent requires satisfaction of certain disclosure an...
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  5.  12
    The Value of Consent for Clinical Research Does Not Always Hinge on Understanding.Neal W. Dickert - 2019 - American Journal of Bioethics 19 (5):20-22.
    Volume 19, Issue 5, May 2019, Page 20-22.
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  6.  21
    Re-Examining Respect for Human Research Participants.Neal W. Dickert - 2009 - Kennedy Institute of Ethics Journal 19 (4):pp. 311-338.
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  7.  9
    The Importance of Listening to Patients and to Evidence Regarding Consent for Research.Neal W. Dickert - 2019 - American Journal of Bioethics 19 (4):23-25.
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  8.  16
    Community Consultation: Not the Problem - an Important Part of the Solution.Neal W. Dickert & Jeremy Sugarman - 2006 - American Journal of Bioethics 6 (3):26 – 28.
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  9.  5
    Patients' Views of Consent in Clinical Trials for Acute Myocardial Infarction: Impact of Trial Design.Neal W. Dickert, Kristopher A. Hendershot, Candace D. Speight & Alexandra E. Fehr - 2017 - Journal of Medical Ethics 43 (8):524-529.
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  10.  3
    A Pragmatic Trial for Emergency Medical Service Providers’ Prehospital Response to Suidality: Consent Is Not Essential, but Limited Patient Engagement May Be Meaningful.Neal W. Dickert - 2019 - American Journal of Bioethics 19 (10):105-107.
    Volume 19, Issue 10, October 2019, Page 105-107.
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  11. Focusing on Partnership in the Context of Limited Decision-Making Capacity.Neal W. Dickert - 2019 - Journal of Law, Medicine and Ethics 47 (4):758-759.
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  12.  3
    Response to Open Peer Commentaries on “Partnering with Patients to Bridge Gaps in Consent for Acute Care Research”.Neal W. Dickert, A. Michelle Bernard, JoAnne M. Brabson, Rodney J. Hunter, Regina McLemore, Andrea R. Mitchell, Stephen Palmer, Barbara Reed, Michele Riedford, Raymond T. Simpson, Candace D. Speight, Tracie Steadman & Rebecca D. Pentz - 2020 - American Journal of Bioethics 20 (8):W12-W13.
    Volume 20, Issue 8, August 2020, Page W12-W13.
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  13.  18
    Does Experience Matter? Implications for Community Consultation for Research in Emergency Settings.Victoria M. Scicluna, Mohammed K. Ali, Rebecca D. Pentz, David W. Wright & Neal W. Dickert - 2017 - Ajob Empirical Bioethics 8 (2):75-81.
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  14.  21
    Uninformed Refusals: Objections to Enrolment in Clinical Trials Conducted Under an Exception From Informed Consent for Emergency Research.Victoria Vorholt & Neal W. Dickert - 2019 - Journal of Medical Ethics 45 (1):18-21.
    Clinical trials in emergency situations present unique challenges, because they involve enrolling individuals who lack capacity to consent in the context of acute illness or injury. The US Department of Health and Human Services and Food and Drug Administration regulations allowing an Exception from Informed Consent in these circumstances contain requirements for community consultation, public disclosure and restrictions on study risks and benefits. In this paper, we analyse an issue raised in the regulations that has received little attention or analysis (...)
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