Outreach, Recruitment, and Education Core


Audience questions drive Ask the Doc community forums.

Achieving the goal of preventing and effectively treating Alzheimer’s by 2025 – as set forth in the National Plan to Address Alzheimer’s Disease – will require partnership between researchers and the community.  The Outreach, Recruitment, and Education (ORE) Core of the UCI ADRC shares knowledge about Alzheimer’s disease in the lay public through a variety of education and outreach activities. Annually, the ORE Core educates over 7,500 individuals about normal aging, MCI, and Alzheimer’s disease.

Annual events include the Southern California Alzheimer’s Disease Research Conference,the quarterly Family Education Series, Ask the Doc community forums, the Barclay Distinguished Lecture series, Behind the Scenes tours, and the ReMIND Symposium.

Dr. Joshua Grill, ORE Core Leader, presents at the 26th Annual Southern California Alzheimer’s Disease Research Conference on October 2, 2015.

A special focus of the ORE Core is outreach to Chinese Americans, who represent a large portion of the Orange County population.  Asian Americans are the fastest growing minority group in the U.S. and few studies are available to instruct potential cultural differences in dementia prevalence, caregiving, attitudes toward diagnosis, or participation in research.  Through culturally tailored educational events and materials, the ADRC engages Asian Americans in research that will  help us better understand cultural differences of dementia.

Effective community collaborations with agencies such as the Alzheimer’s Association, Orange County Chapter, Alzheimer’s Family Services Center, and the Caregiver Resource Center contribute to the success of the ORE Core.  We are particularly grateful to our Community Ambassadors and volunteers who generously give of their time to help represent the ADRC at educational events, health fairs, and other activities.

Click here for more information on the Family Education Series.


Helps families affected by Mild Cognitive Impairment (MCI), Alzheimer's disease, or another dementia while gathering invaluable research data about the clinical presentation and progression of these cognitive disorders.
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Education and Information
Garners community involvement in research, combats the widespread lack of knowledge about Alzheimer’s disease through a variety of education and outreach activities.
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Was it really Alzheimer’s disease? This is the most important question that the Neuropathology Component addresses upon the death of a research volunteer for the children and grandchildren who are concerned about developing dementia.
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Data Management and Statistics
Responsible for transferring our ADRC data to the National Alzheimer’s Coordinating Center which houses and makes available data from all 29 Alzheimer’s disease centers to researchers worldwide.
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Responsible for high-level planning, coordinating the five components and any research projects funded through the ADRC, attracting and nurturing the development of new investigators, and managing all ADRC operational requirements.
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