BID WM Digital Intervention in Aging
Part of paid clinical trials in San Francisco, California.
- Sponsor
- University of California, San Francisco
- Study ID
- NCT06918704
- Status
- Recruiting
Conditions
- Aging
- Inhibitory Control
- Mild Cognitive Impairment (MCI)
- Working Memory
Eligibility Criteria
- Sex
- ALL
- Age
- 60 Years - 85 Years
- Healthy Volunteers
- Accepted
Interventions
- Coherence — BEHAVIORALCoherence is a music-based rhythm training app.
- Worder — BEHAVIORALWorder is a word search app.
Study Details
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.
Key Dates
- Start date
- Aug 15, 2025
- Status verified
- Mar 2026
- Primary completion
- Jan 31, 2028
- Completion
- Jul 31, 2028
Study Design
- Enrollment
- 150 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Coherence InterventionParticipants in this arm will engage with the Coherence Intervention.
- Active Comparator: Worder InterventionParticipants in this arm will engage with the Worder intervention.
Primary Outcome Measure
Working Memory [ Time Frame: Immediately before the intervention, Immediately after the intervention, 6 months after the intervention ]
Central Contacts
- Melissa Arioli(415) 506-7321
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of California, San Francisco | San Francisco | California | 94621 | - |
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