← Eichor
Study identifier: NCT06397469 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Enhancing Attention and Wellbeing Using Digital Therapeutics

Condition: Aging · MCI · Cognitive Decline  ·  Sponsor: University of California, San Francisco

PhaseNA
Planned participants4000
Who can joinAll sexes, 60 Years to 99 Years
Healthy volunteersYes

About this study

The goals of the proposed research are to first determine the minimal and/or optimal dose of a digital intervention required for cognitive enhancement, and then to examine the impact of several potential moderators of treatment effects (i.e., cognitive decline, AD polygenic hazard score, cardiovascular risk, and race/ethnicity). This knowledge gained from his high-impact study with transform the field of cognitive interventions, paving the way for a precision medicine model for cognitive enhancing interventions that improve quality of life for older adults and individuals with cognitive deficits at risk of developing dementia.

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

Talk to the study team

David Ziegler, PhD  ·  4154762164  ·  david.ziegler@ucsf.edu

Monique de Villa, MS, MPH  ·  209-233-3878  ·  meditrain@ucsf.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of California San FranciscoSan Francisco, California, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06397469