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Enhancing Attention and Wellbeing Using Digital Therapeutics

NCT06397469

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

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).

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Aging
  • MCI
  • Cognitive Decline

Eligibility basics and study details

Study type
Interventional
Phase
Not applicable
Ages
60 to 99 years
Sex
All
Healthy volunteers
Accepted
Sponsor
University of California, San Francisco
Last updated on ClinicalTrials.gov
August 24, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 1

  • University of California San Francisco · San Francisco, CA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.