Memory boost study for seniors pulled before start
NCT ID NCT06491264
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to see if personalized, noninvasive brain stimulation could improve working memory in healthy adults aged 50 to 85. Researchers planned to test different stimulation settings and measure brain activity changes. However, the study was withdrawn before any participants were enrolled.
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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.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2027
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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50 to 85 years
- 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: * 50 - 85 y.o. * Endorse good health with no history of mental or physical illness * Willingness to adhere to the study schedule and assessments * Able to read consent document and provide informed consent. * English is a first or primary fluent language. Exclusion Criteria: * Any current psychiatric diagnosis or current Clinical Global Impression ratings of psychiatric illness \> 1 * Neurodevelopmental disorders, history of Central Nervous System (CNS) disease, concussion, overnight hospitalization, or other neurologic sequela, tumors, seizures, meningitis, encephalitis, or abnormal CT or MRI of the brain * Any psychotropic medication is taken within 5 half-lives of procedure time * Any head trauma resulting in loss of consciousness * Visual impairment (except the use of glasses) * Inability to complete cognitive testing * Active participation or plan for enrollment in another evidence-based clinical trial affecting the psychosocial function * Repeated abuse or dependence upon drugs (excluding nicotine and caffeine) or taking medications including stimulants, modafinil, thyroid medication, or steroids * Implanted devices/ferrous metal of any kind * History of seizure or epilepsy, currently taking medications that lower seizure thresholds * Claustrophobia or other conditions that would prevent the MRI assessment. * Pregnancy (or suspected/possible pregnancy or plan to become pregnant in the short term). * Urine Pregnancy Test: If the subject is a woman of childbearing potential and /or a man capable of fathering a child before, during, and/or after participation precautions should be taken. Examples of acceptable methods of birth control for participants involved in the study include birth control pills, patches, Intrauterine Devices (IUD), condoms, sponges, diaphragm with spermicide, or avoiding sexual activity that could cause the subject to become pregnant. * Inability to adhere to the treatment schedule. * Inability to fit the wearable device to the user's head.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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