| Literature DB >> 8820748 |
Abstract
The participation of adolescents in genetic research engenders unusual problems concerning the nature of their informed consent. In this study we analyze 70 consent documents collected from genetics investigators in the United States who conduct research with children and adolescents. We find that many consent documents do not reflect either the current or the developing ethical and legal standards for research with adolescents and that in many cases the documents are simply confusing or unclear. We make recommendations for change to reflect more adequately the changing perspective concerning the autonomous decision-making capacity of adolescents.Entities:
Keywords: Biomedical and Behavioral Research; DHHS Guidelines; Empirical Approach; Genetics and Reproduction
Mesh:
Year: 1995 PMID: 8820748 DOI: 10.1007/bf00995481
Source DB: PubMed Journal: Theor Med ISSN: 0167-9902