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Pediatr Clin North Am. 2008 Feb;55(1):211-22, xii. doi: 10.1016/j.pcl.2007.10.016.

Rethinking pediatric assent: from requirement to ideal.

Author information

1
Division of Hematology/Oncology, Center for Cancer and Blood Disorders, Children's National Medical Center, Washington, DC 20010-2970, USA. yunguru@cnmc.org

Abstract

Physician-investigators are required to obtain informed consent from adult participants in their studies. Inclusion of children in research legally requires informed permission of a child's parent or guardian. It is increasingly recognized that a child need not assume a passive role when included in research, but that his or her active involvement should be sought, as expressed by the child's assent to partake in clinical research. This article briefly explores the history of assent and the central role of assessing a child's understanding of research and preference for participating in decisions related to their care, as necessary components of meaningful assent.

PMID:
18242322
DOI:
10.1016/j.pcl.2007.10.016
[Indexed for MEDLINE]

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