Memory boost in aging with tailored brain stimulation
Official title: Personalized Memory Enhancement in Aging: Pattern-Optimized tACS With Closed-Loop Precision Modulation
Run by Boston University Charles River Campus · NCT07461584 · Data updated 2026-11-12
This study tests whether personalized high-resolution tACS can improve memory in healthy older adults by adjusting stimulation patterns and schedules.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 65 Years and up |
| Sex | All |
| Enrollment | 240 (estimated) |
| Sponsor | Boston University Charles River Campus Academic / other |
| Locations | 1 site (Boston, Massachusetts) |
| Status | Recruiting |
| Started | June 1, 2026 |
| Main results expected | January 31, 2031 |
| Study ends | January 31, 2031 |
| Registry record updated | July 22, 2026 |
| Trial ID | NCT07461584 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 65 and older without dementia or major neurological conditions who meet vision and safety criteria.
✕Probably not a fit
Individuals with significant cognitive impairment, certain implants, or conditions that contraindicate brain stimulation may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Researchers will use multimodal imaging to guide individualized high-resolution tACS aimed at strengthening memory networks in aging adults. The study compares patterned versus continuous stimulation over 1, 3, or 5 consecutive days to see how durability of effects varies. By tracking frontotemporal neural synchrony related to memory processes, the project seeks to optimize when and how long stimulation can help memory in non-demented seniors.
Why it matters
Potential benefit: If successful, participants may experience lasting improvements in memory and a non-drug approach to supporting cognitive health in aging.
How similar studies have gone: Preliminary data suggest that personalized and adaptive brain stimulation can be feasible and may enhance memory, but larger studies are needed for confirmation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 65 years of age or older * normal or corrected-to-normal vision * color vision Exclusion Criteria: * pregnant * metal implants in head * implanted electronic devices * history of neurological problems or head injury * skin sensitivity * claustrophobia * dementia (normal Montreal Cognitive Assessment \> 25) * depression (normal Geriatric Depression Scale \< 10) * history of psychosis * cognitive deficits (MoCA\>25) * any psychoactive medication
Where it's running
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111 Cummington Mall
Boston, Massachusetts, United States Recruiting
Study contacts
- Principal investigator: Robert Reinhart, PhD — Boston University Charles River Campus
- Study coordinator: Robert Reinhart, PhD
- Email: rmgr@bu.edu
- Phone: (617) 353-9481
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.