Literature DB >> 14744301

Should children decide whether they are enrolled in nonbeneficial research?

David Wendler1, Seema Shah.   

Abstract

The U.S. federal regulations require investigators conducting nonbeneficial research to obtain the assent of children who are capable of providing it. Unfortunately, there has been no analysis of which children are capable of assent or even what abilities ground the capacity to give assent. Why should investigators be required to obtain the positive agreement of some children, but not others, before enrolling them in research that does not offer a compensating potential for direct benefit? We argue that the scope of children's research decision making should be based on the principles of respect for autonomy and nonmaleficence. These principles imply that the threshold for assent should be fixed at 14 years of age, and a dissent requirement should be adopted for all children in the context of nonbeneficial research.

Entities:  

Keywords:  Analytical Approach; Biomedical and Behavioral Research; National Commission for the Protection of Human Subjects

Mesh:

Year:  2003        PMID: 14744301     DOI: 10.1162/152651603322614382

Source DB:  PubMed          Journal:  Am J Bioeth        ISSN: 1526-5161            Impact factor:   11.229


  25 in total

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2.  Comparisons of adolescent and parent willingness to participate in minimal and above-minimal risk pediatric asthma research protocols.

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Review 3.  Assent in paediatric research: theoretical and practical considerations.

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5.  Ethics of involving children in health-related research: applying a decision-making framework to a clinical trial.

Authors:  Barbara Kelly; Marilyn J Mackay-Lyons
Journal:  Physiother Can       Date:  2010-10-18       Impact factor: 1.037

6.  Why do children decide not to participate in clinical research: a quantitative and qualitative study.

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7.  Barriers to adolescents' participation in HIV biomedical prevention research.

Authors:  Ralph J DiClemente; Monica S Ruiz; Jessica McDermott Sales
Journal:  J Acquir Immune Defic Syndr       Date:  2010-07       Impact factor: 3.731

8.  Perceptions of parents on the participation of their infants in clinical research.

Authors:  A Gammelgaard; L E Knudsen; H Bisgaard
Journal:  Arch Dis Child       Date:  2006-07-04       Impact factor: 3.791

9.  Children, longitudinal studies, and informed consent.

Authors:  Gert Helgesson
Journal:  Med Health Care Philos       Date:  2005

10.  Body matters: rethinking the ethical acceptability of non-beneficial clinical research with children.

Authors:  Eva De Clercq; Domnita Oana Badarau; Katharina M Ruhe; Tenzin Wangmo
Journal:  Med Health Care Philos       Date:  2015-08
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