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DC Longitudinal Study on Aging and Specimen Bank
Who can join
Ages 45 and older · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Age 45 and older. * Subjects within the age range of 45-50 years old must have a first degree relative with a neurodegenerative disease. Exclusion Criteria: * Individuals under 45 years of age
About the study
The Georgetown University Memory Disorders Program, part of the Department of Neurology, is conducting pilot studies of the feasibility of various diagnostic tests for Alzheimer's disease, mild cognitive impairment and other neurodegenerative diseases. Further, this study is assessing longitudinal changes in biological, lifestyle, and cognitive assessment collection.
The primary goal of this study is to examine the feasibility of biochemical assays, genetic testing, and cognitive and lifestyle assessments in the ante-mortem diagnosis of Alzheimer's disease, mild cognitive impairment and other neurodegenerative diseases. This research involves genetic and cognitive status testing but the findings will not be shared with research subjects. This will be accomplished ex vivo using blood, and/or cerebrospinal fluid (CSF) specimens from patients with a diagnosis of probable Alzheimer's disease, mild cognitive impairment, or other neurodegenerative diseases and from normal controls.
Sponsor: Georgetown University · Participants: 1,000 · Started: Jan 1, 2007
Contact the study team
Official record on ClinicalTrials.gov — NCT03702907
Locations in the U.S.
| District of Columbia | Georgetown University Memory Disorders Program, Washington D.C. |
Conditions
- Alzheimer's Disease
- Dementia
- Mild Cognitive Impairment
- Frontotemporal Dementia
- Lewy Body Dementia
- Vascular Dementia
From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.