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

Account Res. 2007 Oct-Dec;14(4):255-67. doi: 10.1080/08989620701670179.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ethics Committees, Research / organization & administration*
  • Ethics Committees, Research / standards
  • Ethics, Research
  • Guidelines as Topic*
  • Humans
  • Industry
  • Information Dissemination / ethics*
  • Organizational Policy
  • Patient Access to Records / ethics*
  • Patient Access to Records / standards*
  • Research Subjects*
  • Schools, Medical
  • United States
  • Universities