Navigating the maze: ethics approval pathways for intellectual disability research

Document Type

Journal Article

Faculty

Faculty of Health, Engineering and Science

School

School of Medical Sciences / Systems and Intervention Research Centre for Health

RAS ID

16124

Comments

Thomson, A. K., Roberts, P. , & Bittles, A. H. (2013). Navigating the maze: ethics approval pathways for intellectual disability research. Journal of Medical Ethics. Available here

Abstract

All researchers, regardless of their discipline, need to be aware of the importance of protecting vulnerable populations, such as people with intellectual disabilities (ID), from exploitation within the context of research. For this reason, institutional Human Research Ethics Committees (HREC) are regarded as an essential gateway for review of the design and procedure of research projects involving people with ID. While these protections are welcome and necessary, it has been mooted that rigorous application of guidelines of ethical conduct may have a deleterious effect on ID research in Australia. One of the common themes identified by a recent review of the ethical aspects of ID research was the importance of participation, notwithstanding an often reduced capacity for autonomous decision making ‘…that neither the presence of a disability nor the absence of capacity should exclude an individual from participation and that the participation of adults with ID in all research should be pursued.’This paper reviews practical issues arising from a study involving people with ID in Western Australia, and highlights challenges encountered in seeking approval to survey family carers of a group of people with ID. The prescribed involvement of multiple agencies, which was complicated by legislative ambiguities regarding adults who lack the capacity to provide consent for non-medical research participation, resulted in a time span of over 2 years from submission of the initial application to a University HREC to receipt of the final approval for all parts of a project with an original 3-year schedule.

DOI

10.1136/medethics-2012-100899

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