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Abstract
Objective: Prevention trials for neurodegenerative diseases use genetic or other risk marker tests to select participants but there is concern that this could involve coercive disclosure of unwanted information. This has led some trials to use blinded enrollment (participants are tested but not told of their risk marker status). We examined the ethics of blinded vs transparent enrollment using well-established criteria for assessing the ethics of clinical research.
Methods: Normative analysis applying 4 key ethical criteria—favorable risk-benefit ratio, informed consent, fair subject selection, and scientific validity—to blinded vs transparent enrollment, using current evidence and state of Alzheimer disease (AD) and other prevention trials.
Results: Current evidence on the psychosocial impact of risk marker disclosure and considerations of scientific benefit do not support an obligation to use blinded enrollment in prevention trials. Nor does transparent enrollment coerce or involve undue influence of potential participants. Transparent enrollment does not unfairly exploit vulnerable participants or limit generalizability of scientific findings of prevention trials. However, if the preferences of a community of potential participants would affect the rigor or feasibility of a prevention trial using transparent enrollment, then investigators are required by considerations of scientific validity to use blinded enrollment.
Conclusions: Considerations of risks and benefits, informed consent, and fair subject selection do not require the use of blinded enrollment for AD prevention trials. Blinded enrollment in AD prevention trials may sometimes be necessary because of the need for scientific validity, not because it prevents coercion or undue influence.
GLOSSARY
- AD=
- Alzheimer disease;
- IRB=
- institutional review board;
- RCT=
- randomized controlled trial
Footnotes
The views expressed are the authors' and do not represent the positions or policies of the NIH, DHHS, or US government.
Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
- Received October 23, 2014.
- Accepted in final form December 18, 2014.
- © 2015 American Academy of Neurology
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