Literature DB >> 22966027

Views of adolescents and parents on pediatric research without the potential for clinical benefit.

David Wendler1, Emily Abdoler, Lori Wiener, Christine Grady.   

Abstract

OBJECTIVE: Critics argue that pediatric research without the potential for clinical benefit is unethical because it treats children as mere means, exposing those who cannot consent to risks for the benefit of others. The present survey was designed to assess whether this claim is consistent with the views of adolescents who actually participate in research, or their parents.
METHODS: Interviews were conducted with adolescents participating in research at the NIH Clinical Center or Seattle Children's Hospital, and their parents, from June 2008 through April 2010.
RESULTS: Interviews were completed with 177 of 186 adolescent/parent pairs (response rate= 95.2%). Overall, 90% of the adolescents and parents were willing to have the adolescent undergo a few extra blood draws, and 65% were willing to have the adolescent undergo an extra skin biopsy, for research purposes. The vast majority felt that the adolescents were making an important contribution to help others, and 80.8% of the adolescents felt proud to be doing so. Respondents overall were equally willing to have the adolescent face risks to help others in a research study or in a charitable activity.
CONCLUSIONS: The views and experiences of these respondents do not support the claim that pediatric research without the potential for clinical benefit treats subjects as mere means. Instead, the findings provide proof of principle for the claim that non-beneficial pediatric research involves a type of charitable activity which offers children the opportunity to contribute to a valuable project to help others.

Entities:  

Mesh:

Year:  2012        PMID: 22966027      PMCID: PMC3457618          DOI: 10.1542/peds.2012-0068

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  27 in total

1.  Clinical trials in children: problems and pitfalls.

Authors:  R E Kauffman
Journal:  Paediatr Drugs       Date:  2000 Nov-Dec       Impact factor: 3.022

2.  Obtaining informed consent to neonatal randomised controlled trials: interviews with parents and clinicians in the Euricon study.

Authors:  S A Mason; P J Allmark
Journal:  Lancet       Date:  2000-12-16       Impact factor: 79.321

3.  Clinical trials in pediatric cancer: parental perspectives on informed consent.

Authors:  Mary Jo Kupst; Andrea Farkas Patenaude; Gary A Walco; Cheryl Sterling
Journal:  J Pediatr Hematol Oncol       Date:  2003-10       Impact factor: 1.289

4.  Parents' views of their children's participation in phase I oncology clinical trials.

Authors:  Janet A Deatrick; Denise B Angst; Carol Moore
Journal:  J Pediatr Oncol Nurs       Date:  2002 Jul-Aug       Impact factor: 1.636

5.  Voluntary assent in biomedical research with adolescents: a comparison of parent and adolescent views.

Authors:  Janet L Brody; David G Scherer; Robert D Annett; Melody Pearson-Bish
Journal:  Ethics Behav       Date:  2003

Review 6.  Clinical trials in children.

Authors:  Patrina H Y Caldwell; Sharon B Murphy; Phyllis N Butow; Jonathan C Craig
Journal:  Lancet       Date:  2004 Aug 28-Sep 3       Impact factor: 79.321

7.  Parents' attitudes to children's participation in randomized controlled trials.

Authors:  Patrina H y Caldwell; Phyllis N Butow; Jonathan C Craig
Journal:  J Pediatr       Date:  2003-05       Impact factor: 4.406

8.  Risk standards for pediatric research: rethinking the Grimes ruling.

Authors:  David Wendler
Journal:  Kennedy Inst Ethics J       Date:  2004-06

9.  Non-therapeutic research with minors: how do chairpersons of German research ethics committees decide?

Authors:  C Lenk; K Radenbach; M Dahl; C Wiesemann
Journal:  J Med Ethics       Date:  2004-02       Impact factor: 2.903

10.  Parents' and children's attitudes toward the enrollment of minors in genetic susceptibility research: implications for informed consent.

Authors:  Barbara A Bernhardt; Ellen S Tambor; Gertrude Fraser; Lawrence S Wissow; Gail Geller
Journal:  Am J Med Genet A       Date:  2003-02-01       Impact factor: 2.802

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  23 in total

1.  Is Participating in Psychological Research a Benefit, Burden, or Both for Medically Ill Youth and Their Caregivers?.

Authors:  Lori Wiener; Haven Battles; Sima Zadeh; Maryland Pao
Journal:  IRB       Date:  2015 Nov-Dec

2.  Research involving pediatric stem cell donors: A way forward.

Authors:  David Wendler; Nirali N Shah; Michael A Pulsipher; Terry Fry; Christine Grady
Journal:  Clin Trials       Date:  2016-02-17       Impact factor: 2.486

3.  Conducting reproductive research during a new childhood cancer diagnosis: ethical considerations and impact on participants.

Authors:  Leena Nahata; Taylor L Morgan; Keagan G Lipak; Olivia E Clark; Nicholas D Yeager; Sarah H O'Brien; Stacy Whiteside; Anthony N Audino; Cynthia A Gerhardt; Gwendolyn P Quinn
Journal:  J Assist Reprod Genet       Date:  2019-08-01       Impact factor: 3.412

4.  Assent in research: the voices of adolescents.

Authors:  Christine Grady; Lori Wiener; Emily Abdoler; Emily Trauernicht; Sima Zadeh; Douglas S Diekema; Benjamin S Wilfond; David Wendler
Journal:  J Adolesc Health       Date:  2014-03-14       Impact factor: 5.012

Review 5.  Ethics, Emotions, and the Skills of Talking About Progressing Disease With Terminally Ill Adolescents: A Review.

Authors:  Abby R Rosenberg; Joanne Wolfe; Lori Wiener; Maureen Lyon; Chris Feudtner
Journal:  JAMA Pediatr       Date:  2016-12-01       Impact factor: 16.193

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

Authors:  Irma M Hein; Pieter W Troost; Martine C de Vries; Catherijne A J Knibbe; Johannes B van Goudoever; Ramón J L Lindauer
Journal:  Pediatr Res       Date:  2015-04-09       Impact factor: 3.756

7.  Contrasting views of risk perception and influence of financial compensation between adolescent research participants and their parents.

Authors:  Lori Wiener; Adrienne Viola; Benjamin S Wilfond; David Wendler; Christine Grady
Journal:  J Empir Res Hum Res Ethics       Date:  2014-12-17       Impact factor: 1.742

8.  Altruistic reasoning in adolescent-parent dyads considering participation in a hypothetical sexual health clinical trial for adolescents.

Authors:  Noé Rubén Chávez; Camille Y Williams; Lisa S Ipp; Marina Catallozzi; Susan L Rosenthal; Carmen Radecki Breitkopf
Journal:  Res Ethics       Date:  2015-05-27

9.  Perceptions of participating in family-centered fertility research among adolescent and young adult males newly diagnosed with cancer: A qualitative study.

Authors:  Leena Nahata; Taylor L Morgan; Keagan G Lipak; Olivia E Clark; Nicholas D Yeager; Sarah H O'Brien; Stacy Whiteside; Anthony Audino; Gwendolyn P Quinn; Cynthia A Gerhardt
Journal:  Pediatr Blood Cancer       Date:  2019-08-12       Impact factor: 3.167

10.  Adolescent Research Participants' Descriptions of Medical Research.

Authors:  Christine Grady; Isabella Nogues; Lori Wiener; Benjamin S Wilfond; David Wendler
Journal:  AJOB Empir Bioeth       Date:  2015-02-19
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