Zapping the brain to save memory: a new hope for Alzheimer's?
NCT ID NCT07031687
This trial is taking on new participants right now.
First seen Aug 21, 2026 · Last updated Aug 21, 2026
Summary
This trial tests whether a non-invasive technique called temporal interference brain stimulation (TIBS) can improve memory in people with preclinical Alzheimer's disease—those who have early biological signs but no noticeable symptoms. Participants aged 60-80 will receive either active or sham TIBS targeting the hippocampus, a key memory region, for 40 minutes daily over two weeks. Researchers will use brain imaging and EEG to personalize the stimulation and monitor its effects on brain networks and memory up to 12 weeks later.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- Temporal interference brain stimulation (TIBS), a non-invasive brain stimulation technique
- What this could lead to
- If effective, this could offer a non-invasive way to improve memory and slow cognitive decline in people at early risk of Alzheimer's disease.
- What could go wrong
- This is an early-stage trial, and the effects on memory are uncertain. The stimulation may not produce lasting benefits, and there could be unknown side effects.
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 1,200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Dec 2029
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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60 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Individuals recruited from neurology memory clinics or communities. * Age between 60 and 80 years old, inclusive; no gender limitation. * Right-handed. * Cognitive function test results within normal range after age, gender, and education-level adjustment, OR mild cognitive impairment not yet meeting diagnostic criteria for Mild Cognitive Impairment (MCI), OR only subjective cognitive decline. * Individuals classified as preclinical AD based on the revised 2024 AD diagnostic and staging criteria (i.e., cognitively normal with positive plasma p-tau217 or positive Aβ PET). * Full understanding of the study, voluntary participation, and provision of written informed consent approved by the Ethics Committee. Exclusion Criteria: * Past or present neurological diseases (e.g., stroke, epilepsy, Parkinson's disease, multiple sclerosis). * Psychiatric disorders such as severe depression or severe anxiety. * Systemic diseases causing cognitive decline (e.g., severe thyroid dysfunction, severe liver or kidney disease, severe nutritional deficiencies). * Currently taking medications that may affect cognitive function (e.g., anticholinergics, benzodiazepines, antipsychotics) that cannot be discontinued or adjusted. * Other factors leading to cognitive decline that are not AD-related. * Contraindications for MRI scans, such as claustrophobia, implanted metallic devices (e.g., pacemakers, cochlear implants, aneurysm clips), or history of head injury with retained metal fragments.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hainan university
RECRUITINGSanya, Hainan, China
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Xuanwu Hospital of Capital Medical University
RECRUITINGBeijing, China
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