Literature DB >> 8820748

Genetic research, adolescents, and informed consent.

R F Weir1, J R Horton.   

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


  40 in total

1.  Children's dissent to research--a minor matter?

Authors:  Gregory E Pence
Journal:  IRB       Date:  1980-12

2.  DNA banking and informed consent -- part 1.

Authors:  Robert F Weir; Jay R Horton
Journal:  IRB       Date:  1995 Jul-Aug

3.  Guidelines for adolescent participation in research: current realities and possible resolutions.

Authors:  Audrey Smith Rogers; Lawrence D'Angelo; Donna Futterman
Journal:  IRB       Date:  1994 Jul-Aug

4.  Genetics and just health care: a Genome Task Force report.

Authors:  T H Murray
Journal:  Kennedy Inst Ethics J       Date:  1993-09

5.  The consent process and children.

Authors:  M E Broome; K A Stieglitz
Journal:  Res Nurs Health       Date:  1992-04       Impact factor: 2.228

6.  Rights to privacy in research: adolescents versus parents.

Authors:  Jeanne Brooks-Gunn; Mary Jane Rotheram-Borus
Journal:  Ethics Behav       Date:  1994

7.  Additional protections for children involved as subjects in research--Department of Health and Human Services. Final rule.

Authors: 
Journal:  Fed Regist       Date:  1983-03-08

8.  Whose DNA is it anyway? Relationships between families and researchers.

Authors:  V L Hannig; E W Clayton; K M Edwards
Journal:  Am J Med Genet       Date:  1993-08-15

9.  The introduction of cystic fibrosis carrier screening into clinical practice: policy considerations.

Authors:  B S Wilfond; N Fost
Journal:  Milbank Q       Date:  1992       Impact factor: 4.911

10.  Consent for minors to participate in nontherapeutic research.

Authors:  T G Furlow
Journal:  Leg Med       Date:  1980
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  2 in total

1.  Enhancing the ethical conduct of genetic research: investigating views of parents on including their healthy children in a study on mild hearing loss.

Authors:  L Gillam; Z Poulakis; S Tobin; M Wake
Journal:  J Med Ethics       Date:  2006-09       Impact factor: 2.903

2.  Consent procedures in pediatric biobanks.

Authors:  Noor Aa Giesbertz; Annelien L Bredenoord; Johannes Jm van Delden
Journal:  Eur J Hum Genet       Date:  2014-12-24       Impact factor: 4.246

  2 in total

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