Literature DB >> 18246944

Offering results to research subjects: U.S. Institutional Review Board policy.

Christa Kozanczyn1, Katie Collins, Conrad V Fernandez.   

Abstract

BACKGROUND: This study aims to determine the nature of United States Institutional Review Board (IRB) policy in a broad spectrum of research settings regarding the return of results to study participants.
METHOD: IRB policies or standard operating procedures of 207 Medical School, Industry and Non-medical School IRBs were examined on-line to determine if they incorporated specific reference to the return of results to participants at the conclusion of the research.
RESULTS: The majority of IRBs had no available policy regarding the return of research results to participants [56% (n = 116)]. A further third 136.3% (n = 75)] had policies that were defined as vague or that only indirectly mentioned the return of results. Medical School IRBs were more likely to have a policy than Industry or Non-medical University IRBs, respectively (odds ratio, 4.63; 95% confidence interval, 1.84 to 11.66 and odds ratio, 3.03; 95 % confidence interval, 1.75 to 5.25). Few provided any guidance as to the process of return of results. Of the IRBs that had a research results policy, 54.9% (n = 50) specifically addressed genetic research.
CONCLUSIONS: Our findings demonstrate a marked lack of uniformity in IRB policy regarding the return of study results with over half providing no guidance.

Entities:  

Mesh:

Year:  2007        PMID: 18246944     DOI: 10.1080/08989620701670179

Source DB:  PubMed          Journal:  Account Res        ISSN: 0898-9621            Impact factor:   2.622


  13 in total

1.  Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility.

Authors:  Christopher A Cassa; Sarah K Savage; Patrick L Taylor; Robert C Green; Amy L McGuire; Kenneth D Mandl
Journal:  Genome Res       Date:  2012-01-06       Impact factor: 9.043

2.  Utilizing Focus Groups with Potential Participants and Their Parents: An Approach to Inform Study Design in a Large Clinical Trial.

Authors:  Sandeep Kadimpati; Jennifer B McCormick; Yichen Chiu; Ashley B Parker; Aliya Z Iftikhar; Randall P Flick; David O Warner
Journal:  AJOB Empir Bioeth       Date:  2014-01-01

3.  Return of Genetic Research Results to Participants and Families: IRB Perspectives and Roles.

Authors:  Laura M Beskow; P Pearl O'Rourke
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

4.  Canadian Research Ethics Board Leadership Attitudes to the Return of Genetic Research Results to Individuals and Their Families.

Authors:  Conrad V Fernandez; P Pearl O'Rourke; Laura M Beskow
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

Review 5.  Burdens on research imposed by institutional review boards: the state of the evidence and its implications for regulatory reform.

Authors:  George Silberman; Katherine L Kahn
Journal:  Milbank Q       Date:  2011-12       Impact factor: 4.911

6.  Researcher practices on returning genetic research results.

Authors:  Christopher Heaney; Genevieve Tindall; Joe Lucas; Susanne B Haga
Journal:  Genet Test Mol Biomarkers       Date:  2010-10-12

7.  Informed consent and genomic incidental findings: IRB chair perspectives.

Authors:  Christian M Simon; Janet K Williams; Laura Shinkunas; Debra Brandt; Sandra Daack-Hirsch; Martha Driessnack
Journal:  J Empir Res Hum Res Ethics       Date:  2011-12       Impact factor: 1.742

8.  IRB chairs' perspectives on genotype-driven research recruitment.

Authors:  Laura M Beskow; Emily E Namey; Patrick R Miller; Daniel K Nelson; Alexandra Cooper
Journal:  IRB       Date:  2012 May-Jun

9.  Recommendations for the return of research results to study participants and guardians: a report from the Children's Oncology Group.

Authors:  Conrad V Fernandez; Kathleen Ruccione; Robert J Wells; Jay B Long; Wendy Pelletier; Mary C Hooke; Rebecca D Pentz; Robert B Noll; Justin N Baker; Maura O'Leary; Gregory Reaman; Peter C Adamson; Steven Joffe
Journal:  J Clin Oncol       Date:  2012-10-29       Impact factor: 44.544

10.  Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.

Authors:  Lainie Friedman Ross; Ellen Wright Clayton
Journal:  Pediatrics       Date:  2019-11-12       Impact factor: 7.124

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