The Comparative Effectiveness Dementia & Alzheimer's Registry (CEDAR)
This study, called The Comparative Effectiveness Dementia & Alzheimer's Registry (CEDAR), is looking at how well different treatments work for Alzheimer's disease (AD) and mild cognitive impairment (MCI). It's an observational study, meaning researchers will watch what happens during your routine medical care. You might receive individualized evidence-based multidomain interventions (education, medications, and non-medication approaches). The study aims to see if these interventions can improve your thinking and memory. Researchers will measure changes in your cognitive (thinking) abilities every six months for 18 months. You can join if you are 18 or older and have a family history of Alzheimer's, memory concerns, or a diagnosis of MCI or early AD. The study is currently unclear on its recruitment status and plans to include about 452 people.
- Study design
- This is an observational study, meaning researchers will collect information during your regular medical care. It aims to include about 452 participants.
- What's involved
- Participants will receive individualized evidence-based multidomain interventions as part of their routine outpatient clinical care. Your cognitive abilities will be measured every 6 months.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your cognitive abilities will be measured for 18 months after starting the study.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
The Comparative Effectiveness Dementia & Alzheimer's Registry
At a glance
Conditions
NCT03687710
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Weill Cornell Medicine
New York, New Yorkno site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Schantel Williams, MPH, RN · PRINCIPAL_INVESTIGATOR · Program Director of Alzheimer's Prevention Program
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
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Inclusion
Exclusion
What this trial measures
- Change from Baseline in Alzheimer's Prevention Initiative Cognitive Composite (APCC) every 6 monthsevery 6 months, for 18 months
Composite Cognitive Battery (including NIH Toolbox Cognition Battery and other pen-and-paper neuropsychological tests).