Home › Mild Cognitive Impairment › NCT06918704
BID WM Digital Intervention in Aging
Behavioral Intervention Development Core - Working Memory Digital Intervention in Aging
Who can join
Ages 60 to 85 · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Minimum of 12 years of education * English fluency * Normal or corrected-to-normal vision * Normal or corrected-to-normal vision * Medically healthy older adults including those with below-average cognitive performance or mild cognitive impairment patients without dementia Exclusion Criteria: * Under the age of 60 * Clinical diagnosis of neurological or psychiatric disorder * Visually or hearing impaired without correction to normal * Clinical diagnosis of dementia or AD8 score of \>3 * Regularly (one or more times per week) practicing an instrument within the last year * 10 or more years of formal musical instrument training
About the study
The goal of this clinical trial is to learn if engaging with an digital intervention may improve cognitive function. The main questions it aims to answer are:
1. Does engagement in with a digital intervention improve working memory? 2. Does engagement in with a digital intervention improve inhibitory control?
Researchers will compare two different digital interventions to assess whether they may be helpful in improving cognitive function.
Participants will conduct study activities remotely (e.g., at-home):
1. Baseline Assessment. Complete a series of cognitive assessments and surveys. 2. Intervention. Engage in a digital intervention for up to 8 weeks. 3. Post Intervention Assessment. Complete the same cognitive assessments and surveys as the Baseline Assessment. 4. Follow-Up Assessment. Six months after the intervention ends, participants will complete the same cognitive assessments and surveys as the Baseline Assessment.
What is being tested
- Coherence (behavioral)
- Worder (behavioral)
Sponsor: University of California, San Francisco · Participants: 150 · Started: Aug 15, 2025
Contact the study team
- Melissa Arioli · Phone: (415) 506-7321
Official record on ClinicalTrials.gov — NCT06918704
Locations in the U.S.
| California | University of California, San Francisco, San Francisco |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.