DIGITAL Biomarker: Blood Based Biomarkers in the Primary Care Setting for Alzheimer's Disease
Completed
Conditions studied: Mild Cognitive Impairment
In brief
The primary objective of this study is to evaluate the feasibility of implementing blood-based biomarker testing for amyloid positivity designed to aid the early detection of Alzheimer's Disease and Related Dementia (ADRD) in patients 65+ including the rate that patients and providers follow up abnormal blood-based biomarker testing.
Key facts
- Study ID
- NCT05844488
- Run by
- Indiana University
- People needed
- 26
- Starts
- 2023-03-31
- Expected to finish
- 2023-06-30
- Last updated by the study team
- 2023-07-25
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients must be > 65 years of age
- Any gender
- Is an established or new patient at one of the 6 participating IUHP PC sites
- Is able to provide informed consent (research portion only for the biomarker consent) or has a Legally Authorized Representative (LAR) who can provide informed consent
- Has a "red" DCA screening in the last 12 months (a score of 0 or 1 out of 5)
You may not qualify if…
- Patients who do not complete a DCA screening for any reason
- Existing diagnosis of dementia documented in their medical record based on ICD-10 codes
Where it is running
- Indiana University Health Physicians Primary Care — Indianapolis, Indiana, United States
Full record on ClinicalTrials.gov
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