Zapping the brain to preserve memory — a precision approach puts it to the test
NCT ID NCT07722598
First seen Jul 23, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This trial tests whether a noninvasive technique called transcranial alternating current stimulation (tACS) can improve working memory in healthy adults aged 65 and older. The stimulation is personalized to each person's unique brain rhythms and delivered through electrodes on the scalp. Researchers aim to see if this drug-free approach can strengthen the brain networks that support memory.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- personalized transcranial alternating current stimulation (tACS) tailored to individual brain rhythms
- What this could lead to
- If it works, this could lead to a drug-free way to sharpen memory in older adults and help delay age-related cognitive decline.
- What could go wrong
- This is an early-stage trial testing brain stimulation in healthy volunteers; effects may be small or not translate to real-world memory benefits, and individual responses can vary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 160 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2028
An estimate. Start dates often move.
- Expected to finish
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Jan 2031
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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