The Comparative Effectiveness Dementia & Alzheimer's Registry
Part of paid clinical trials in New York, New York.
- Sponsor
- Weill Medical College of Cornell University
- Study ID
- NCT03687710
- Status
- Enrolling By Invitation
Conditions
- Alzheimer Disease
- Mild Cognitive Impairment
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 99 Years
- Healthy Volunteers
- Accepted
Interventions
- Multidomain precision medicine intervention — BEHAVIORALParticipants will receive individualized evidence-based multidomain interventions (education, pharmacologic, non-pharmacologic) in the setting of routine outpatient clinical care.
Study Details
To evaluate the effectiveness of using clinical precision medicine to develop lifecourse interventions for Alzheimer's disease (AD) prevention and treatment. Anthropometrics, blood biomarkers (including genetics), and cognition will measured longitudinally to assess the comparative effectiveness of clinical care.
Key Dates
- Start date
- Feb 16, 2015
- Status verified
- Mar 2026
- Primary completion
- Jun 30, 2028
- Completion
- Jun 30, 2028
Study Design
- Enrollment
- 452 participants (estimated)
Primary Outcome Measure
Change from Baseline in Alzheimer's Prevention Initiative Cognitive Composite (APCC) every 6 months [ Time Frame: every 6 months, for 18 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Weill Cornell Medicine | New York | New York | 10021 | - |
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