Nothing about us without us? Using public consensus for priority setting in Alzheimer's disease research.
Timothy Daly1,2
1Bioethics Program, FLACSO Argentina, Buenos Aires, Argentina.
Journal of Alzheimer'S Disease : JAD
|January 20, 2026
Summary
Engaging the public in Alzheimer's disease and related dementias research priority setting ensures studies address societal needs. This involvement makes research more impactful for those affected by these conditions.
Area of Science:
- Neuroscience
- Public Health
- Health Services Research
Background:
- Alzheimer's disease and related dementias (AD/ADRD) research requires public input for greater relevance.
- Current research priorities may not fully align with the needs of affected communities.
Purpose of the Study:
- To emphasize the necessity of public involvement in setting research priorities for AD/ADRD.
- To advocate for research questions that address societal concerns and values.
Main Methods:
- Review of current practices in research priority setting.
- Analysis of the impact of public engagement in health research.
Main Results:
- Public involvement in upstream consensus-building enhances research impact.
- Societal relevance is a critical factor for impactful AD/ADRD research.
Conclusions:
- Integrating public perspectives into AD/ADRD research priority setting is crucial.
- Future research should prioritize questions reflecting societal values and concerns.
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