Actively Recruiting
BID WM Digital Intervention in Aging
Led by University of California, San Francisco · Updated on 2026-04-01
150
Participants Needed
1
Research Sites
154 weeks
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
N
National Institute on Aging (NIA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
BID WM Digital Intervention in Aging
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Minimum of 12 years of education
- English fluency
- Normal or corrected-to-normal vision
- Medically healthy older adults including those with below-average cognitive performance or mild cognitive impairment patients without dementia
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of California, San Francisco
San Francisco, California, United States, 94621
Actively Recruiting
Research Team
M
Melissa Arioli
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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