Original Article
A neuroimaging proof of principle study of Down's syndrome and dementia: ethical and methodological challenges in intrusive research
Article first published online: 2 NOV 2011
DOI: 10.1111/j.1365-2788.2011.01495.x
© 2011 The Authors. Journal of Intellectual Disability Research © 2011 Blackwell Publishing Ltd
Issue

Journal of Intellectual Disability Research
Special Issue: Mental Health and Intellectual Disability: XXIXII
Volume 57, Issue 2, pages 105–118, February 2013
Additional Information
How to Cite
d'Abrera, J. C., Holland, A. J., Landt, J., Stocks-Gee, G. and Zaman, S. H. (2013), A neuroimaging proof of principle study of Down's syndrome and dementia: ethical and methodological challenges in intrusive research. Journal of Intellectual Disability Research, 57: 105–118. doi: 10.1111/j.1365-2788.2011.01495.x
Publication History
- Issue published online: 4 JAN 2013
- Article first published online: 2 NOV 2011
- Accepted 12 September 2011
- Abstract
- Article
- References
- Cited By
Keywords:
- Alzheimer's disease;
- amyloid;
- Down's syndrome;
- ethics;
- intellectual disabilities;
- intrusive research
Abstract
Background Research into specific illnesses and the development of new treatments may only become possible as new technologies become available. When used for research, such technologies may best be described as ‘intrusive’, in that they require a considerable willingness and commitment on the part of the participants. This has increasingly been the case for brain disorders and illnesses where novel neuroimaging techniques, often combined with clinical and psychological assessments, have the potential to result in new understanding. People with intellectual disabilities (ID) have a history of under-representation as participants in research using such technologies and are therefore at risk of not receiving equal access to state-of-the-art treatments. We propose that ‘intrusive’ biomedical research is both possible and ethical in ID, and explore some of the methodological challenges by reference to a recent proof of principle study that used a relatively new ligand-based brain scanning technique in a group of volunteers with Down's syndrome.
Methods Five overlapping stages of the study methodology were identified and evaluated for their acceptability to volunteers with mild to moderate ID through discussion, reflection, and analysis of structured feedback in the context of key policy documents, ethical guidelines and relevant legislation.
Results Identification of key ethical and methodological challenges from reflective practice and participant feedback facilitated the emergence of strategies that permitted continual refinement of the study design. Important areas considered included (1) being clear about the purpose and scientific justification for the study; (2) reconciling the potential risks and benefits with relevant ethical guidelines and legislation; (3) identifying and implementing effective recruitment strategies; (4) optimising and assessing capacity to consent; and (5) making the ‘intrusive’ procedures as acceptable as possible to people with ID.
Conclusion We were able to demonstrate that a proof of principle study incorporating a novel brain scanning technique in a group of volunteers with ID was feasible, safe and well tolerated, despite the vulnerabilities of the study cohort and the intrusive nature of the research. We consider the study within an ethical and historical discourse about the principles that define current ‘best practice’ in ID research and propose a number of key recommendations for making intrusive research acceptable in people with ID.

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