DC Longitudinal Study on Aging and Specimen Bank

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 45
Healthy Volunteers: t
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• Age 45 and older.

• Subjects within the age range of 45-50 years old must have a first degree relative with a neurodegenerative disease.

Locations
United States
Washington, D.c.
Georgetown University Memory Disorders Program
RECRUITING
Washington D.c.
Time Frame
Start Date: 2007-01-01
Estimated Completion Date: 2027-01
Participants
Target number of participants: 1000
Treatments
Normal Cognition
No diagnosis of a cognitive disorder
Cognitive Disorder
Diagnosed with a cognitive disorder such as :Mild Cognitive Impairment, Alzheimer's disease, Frontotemporal Dementia, Lewy Body Dementia, Vascular Dementia, or other neurodegenerative condition.
Sponsors
Leads: Georgetown University

This content was sourced from clinicaltrials.gov