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Study identifier: NCT07516119 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Predicting Pre-dementia

Condition: Mild Cognitive Impairment (MCI) · Alzheimer Dementia (AD) · Alzheimer Disease (AD)  ·  Sponsor: Prevention Research Consortium Corp.

PhaseN/A
Planned participants100
Who can joinAll sexes, 55 Years to no upper limit
Healthy volunteersYes

About this study

The goal of this observational study is to learn how well a multimodal "Progression and Risk" (PR) model can predict and stage early mild cognitive impairment (MCI) due to Alzheimer's disease in cognitively normal or very mildly impaired ApoE4-positive adults aged 55 and older. The main questions it aims to answer are: Can a prespecified proteogenomic PR model accurately predict conversion from cognitively normal (CN) or very mildly impaired status to pTau217-positive MCI Stage I within 24 months in ApoE4-positive adults? Does adding digital monitoring features (e.g., sleep, activity, speech), EMR-lifestyle risk scores, and plasma biomarkers to a polygenic risk score (PRS) meaningfully improve risk stratification and time-to-conversion prediction compared with simpler models (e.g., PRS alone or standard clinical risk factors)? If there is a comparison group: Researchers will compare performance of the full multimodal PR model (integrating PRS, plasma proteomics and other omics, digital monitoring, and EMR-lifestyle data) with simpler or reduced models (for example, PRS-only, biomarker-only, or models without continuous digital monitoring) to see if the full model provides higher discrimination (AUC/ROC), better calibration, and improved time-to-conversion prediction for CN to pTau217-positive MCI transitions. Participants will: Provide prior genomic data (ApoE genotype and whole-genome sequencing or high-density genotyping array data) for calculation of an ancestry- and …

This description comes directly from the study's public registry record.

Talk to the study team

Foster Carr, MD  ·  8772716078  ·  drcarr@prevention-research.org

Always discuss trial participation with your own doctor first.

Locations (1)

Foster Carr MDSan Diego, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07516119