20 found

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  1.  22
    The Ethics of Net‐Risk Pediatric Research: Implications of Valueless and Harmful Studies.Wendler David - 2018 - IRB: Ethics & Human Research 40 (6):13-18.
    Net‐risk pediatric research encompasses interventions and studies that pose risks and do not offer a compensating potential for clinical benefit. These interventions and studies are central to efforts to improve pediatric clinical care. Yet critics argue that it is unethical to expose children to research risks for the benefit of unrelated others. While a number of ethical justifications have been proposed, none have received widespread acceptance. This leaves funders with uncertainty over whether they should support and institutional review boards with (...)
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  2.  18
    Financial Payments for Participating in Research while Incarcerated: Attitudes of Prisoners.Ravi Divya, Paul P. Christopher, Eliza J. Filene, Sarah Ailleen Reifeis & Becky L. White - 2018 - IRB: Ethics & Human Research 40 (6):1-6.
    The practice of paying prisoners to for their participation in research has long been debated, and the controversy is reflected in the differing policies in the U.S. prison systems. Empirical study of financial payments to inmates who enroll in research has focused on whether this practice is coercive. In this study, we examined whether monetary incentives have the potential to be unduly influential among fifty HIV‐positive prisoners. The majority of prisoners surveyed believed that inmates should receive some compensation for their (...)
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  3.  22
    Broad Consent for Future Research: International Perspectives.Mark A. Rothstein, Heather L. Harrell, Katie M. Saulnier, Edward S. Dove, Chien Te Fan, Tzu-Hsun Hung, Obiajulu Nnamuchi, Alexandra Obadia, Gil Siegal & Bartha Maria Knoppers - 2018 - IRB: Ethics & Human Research 40 (6):7-12.
    In the United States, final amendments to the Federal Policy for the Protection of Human Subjects (“the Common Rule”) were published on January 19, 2017, and they will take effect on January 21, 2019. One of the most widely discussed provisions is that for the first time, federal regulations governing research with humans authorize the use of broad consent for future, unspecified research on individually identifiable biospecimens and associated data. Many questions have been raised about broad consent, including what effect (...)
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  4.  11
    Advance Directives for Research: How Do They Compare with Surrogates’ Predictions of Older Adults’ Preferences?Élodie Hérault, Gina Bravo & Lise Trottier - 2018 - IRB: Ethics & Human Research 40 (5):11-19.
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  5.  19
    Promoting Research with Organ Transplant Patients.Sarah R. Lieber, Thomas D. Schiano & Rosamond Rhodes - 2018 - IRB: Ethics & Human Research 40 (5):1-10.
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  6.  24
    The Need to Track Payment Incentives to Participate in HIV Research.Brandon Brown, Jerome T. Galea, Karine Dubé, Peter Davidson, Kaveh Khoshnood, Lisa Holtzman, Logan Marg & Jeff Taylor - 2018 - IRB: Ethics & Human Research 40 (4):8-12.
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  7.  16
    Potential Benefits to Families, Children, and Adolescents, Enrolled in Longitudinal Qualitative Research.Minisha Lohani, Kristopher A. Hendershot, Wendy Pelletier, Kristin Stegenga, Margie Dixon, Pamela Hinds, Melissa A. Alderfer & Rebecca D. Pentz - 2018 - IRB: Ethics & Human Research 40 (4):1-7.
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  8.  12
    Therapeutic Misperceptions in Early‐Phase Cancer Trials: From Categorical to Continuous.Bryan A. Sisk & Eric Kodish - 2018 - IRB: Ethics & Human Research 40 (4):13-20.
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  9.  19
    Against Consent Form Language Requiring Multiple or Specific Methods of Contraception.Mark G. Kuczewski & Emily E. Anderson - 2018 - IRB: Ethics & Human Research 40 (3):11-13.
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  10.  12
    Ethical Issues in the Use of Nudges to Obtain Informed Consent for Biomedical Research.Maxwell J. Mehlman, Eric Kodish & Jessica Berg - 2018 - IRB: Ethics & Human Research 40 (3):1-5.
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  11.  15
    A Study of Reliance Agreement Templates Used by U.S. Research Institutions.David B. Resnik, Juliet Taylor, Kathryn Morris & Shi Min - 2018 - IRB: Ethics & Human Research 40 (3):6-10.
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  12.  14
    Implementing Single IRB Review of Multisite Research: Lessons Learned from the National Children’s Study.Julia Slutsman, Nancy Dole, Steven Leuthner & Mark S. Schreiner - 2018 - IRB: Ethics & Human Research 40 (3):14-20.
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  13.  9
    Moving from the “Why” to the “How”: Two Approaches to Including Research Participants’ Voices.Stephanie Solomon Cargill - 2018 - IRB: Ethics & Human Research 40 (2):8-11.
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  14.  15
    Experimentation without Representation.Rebecca Dresser - 2018 - IRB: Ethics & Human Research 40 (2):3-7.
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  15.  15
    Power Concedes Nothing without a Demand: The Case for a Patient Boycott of U.S. Clinical Trials.Carl Elliott - 2018 - IRB: Ethics & Human Research 40 (2):15-18.
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  16.  23
    Research with Human Subjects: Humility and Deception.Nancy M. P. King - 2018 - IRB: Ethics & Human Research 40 (2):12-14.
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  17.  8
    Making Voices Matter.Karen J. Maschke - 2018 - IRB: Ethics & Human Research 40 (2):1-2.
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  18.  31
    Patient‐Centered Outcomes Research: Stakeholder Perspectives and Ethical and Regulatory Oversight Issues.Emily A. Largent, Joel S. Weissman, Avni Gupta, Melissa Abraham, Ronen Rozenblum, Holly Fernandez Lynch & I. Glenn Cohen - 2018 - IRB: Ethics & Human Research 40 (1):7-17.
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  19.  19
    Presurgical Trials: Ethical Pitfalls of a Novel Research Method.Myrick C. Shinall & Anji Wall - 2018 - IRB: Ethics & Human Research 40 (1):1-6.
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  20.  14
    The Food and Drug Administration’s Federal Review of a Pediatric Muscular Dystrophy Protocol.Donna L. Snyder & Robert M. Nelson - 2018 - IRB: Ethics & Human Research 40 (1):18-20.
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