DO NOT DELETE BETWEEN THESE LINES
DO NOT DELETE BETWEEN THESE LINES
In April 2020, DC Health partnered with the GW Institute for Brain Health and Dementia to conduct a Brain Health Needs Assessment for the District of Columbia. The objectives of the project were to:
- Estimate the prevalence of dementia in DC
- Estimate the prevalence of modifiable risk factors for cognitive decline and dementia in DC
- Identify challenges and unmet needs of caregivers for persons living with dementia in DC
- Develop a guide identifying services and resources available to DC residents related to the needs of persons living with dementia and their caregivers
The completed report and guide identifying services and resources are available in the links below.
- District of Columbia: 2020 Brain Health Needs Assessment
- Services and Resources for Memory Loss and Dementia Care
Behavioral Risk Factor Surveillance System (BRFSS)
The Behavioral Risk Factor Surveillance System (BRFSS) is the nation’s premier system of telephone surveys that collect state-level data about health risk behaviors, chronic health conditions, and use of preventive services.
Subjective Cognitive Decline (SCD)
Subjective Cognitive Decline (SCD) is the self-reported experience of worsening or more frequent confusion or memory loss. SCD can have implications for living with and managing chronic diseases or performing daily activities like cooking or cleaning. Because SCD is self-reported, it does not imply a diagnosis of cognitive decline by a health care professional.
- Washington DC: Subjective Cognitive Decline
- National Data | Spanish (Español)
- African American Adults | Spanish (Español)
- American Indian/Alaska Native Adults | Spanish (Español)
- Asian/Pacific Islander Adults | Spanish (Español)
- Hispanic Adults | Spanish (Español)
- Women | Spanish (Español)
- Men | Spanish (Español)
- Lesbian, Gay, Bisexual, Transgender(LGBT) Adults | Spanish (Español)
- Veterans | Spanish (Español)
To learn more, visit Subjective Cognitive Decline — A Public Health Issue
Caregiving Data
BRFSS Caregiver module is an important tool for collecting public health data on informal or unpaid caregivers who provide regular care or assistance to family and friends with chronic illnesses or disability conditions.
- Washington DC: Caregiver Data
- National Data
- African American Adults | Spanish (Español)
- American Indian/Alaska Native Adults | Spanish (Español)
- Asian/Pacific Islander Adults | Spanish (Español)
- Hispanic Adults | Spanish (Español)
- Women |Spanish (Español)
- Men |Spanish (Español)
- Lesbian, Gay, Bisexual, Transgender (LGBT) Adults | Spanish (Español)
- Veterans | Spanish (Español)
To learn more, visit Caregiving for Family and Friends — A Public Health Issue.