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Federal Efforts to Address Racial and Ethnic Disparities in Alzheimer’s Disease and Related Dementias

Publication Date
Authors
Emma Nye, Helen Lamont, Lauren Anderson

The National Alzheimer’s Project Act (NAPA) requires “the inclusion of ethnic and racial populations at higher risk for Alzheimer's or least likely to receive care, in clinical, research, and service efforts with the purpose of decreasing health disparities in Alzheimer's”.1 In order to meet this requirement, in 2020 the Advisory Council on Alzheimer’s Research, Care, and Services recommended that in order to advance health equity, work must be done to address racial and ethnic disparities in Alzheimer’s disease and related dementias (ADRD). As a starting point, the Advisory Council tasked the U.S. Department of Health and Human Services (HHS) to develop a report on federal initiatives taken to address such disparities. The Office of the Assistant Secretary for Planning and Evaluation (ASPE), which coordinates the implementation of NAPA, developed the following issue brief and inventory of federal efforts to address racial and ethnic disparities in dementia research, care, and services.

*This content is in the process of Section 508 review. If you need immediate assistance accessing this content, please submit a request to Brenda Veazey, (202) 260-6158, brenda.veazey@hhs.gov. Content will be updated pending the outcome of the Section 508 review.

Product Type
ASPE Issue Brief
Populations
Older Adults | Black & African American People | American Indian & Alaska Native People (AI-AN) | Asian American & Pacific Islanders People (AAPI) | Hispanic, Latino, Latina, & Latinx People | Racial & Ethnic Groups | Caregivers | Low-Income Populations | Medicare Beneficiaries | People Living with Dementia | Underserved Populations