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Zapping the brain to sharpen memory: new trial tests TMS in older adults
NCT ID NCT03574207
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This pilot study tests whether a non-invasive brain stimulation technique called transcranial magnetic stimulation (TMS) can improve memory in healthy adults and in older adults with amnestic mild cognitive impairment (aMCI), a condition that often leads to Alzheimer's. Researchers will use face-word association tasks and brain scans to measure changes. The study enrolls 48 participants across three groups: young adults, healthy older adults, and those with aMCI.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcranial magnetic stimulation (TMS)
- What this could lead to
- If it works, this could point toward a non-invasive treatment to improve memory in people with mild cognitive impairment.
- What could go wrong
- This is a small, early pilot study. Results may not generalize, and memory improvements may be modest or not lasting.
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 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2019
- 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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19 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.
The investigators anticipate enrolling 48 subjects total: * 16 healthy young adults (age 19-35) * 16 healthy older adults (demographically matched to aMCI group for age, sex, and educational attainment) * 16 older adults diagnosed with amnestic mild cognitive impairment (aMCI) Inclusion Criteria: 1. Adults 19 years of age and older 2. Healthy adults without history of psychiatric or neurological disease OR previous diagnosis of amnestic MCI 3. Must be able to provide informed consent 4. Must have the ability to comply with basic instructions and have the ability to sit comfortably still for TMS, neuroimaging, and other study procedures. 5. Right-handed based on self-report (pre-screening) and evaluation with a standard test. Exclusion Criteria: 1. Individuals who have ferrous metal implanted in their body (other than in their teeth) or any other non-removable medical and/or metallic implant 2. Individuals who have increased intracranial pressure 3. Individuals who have any major medical illness (e.g., cancer, HIV+, hepatitis, heart disease) 4. Individuals who have confounding/dual diagnoses (e.g., comorbid mental illness and substance use disorder) 5. Individuals with current diagnoses of alcohol or substance abuse/dependence 6. Individuals with epilepsy, any history of seizures, or using medication that lowers seizure threshold 7. Individuals with any neurological disorder other than aMCI (e.g., stroke, traumatic brain injury) 8. Pregnant females --- as determined by urine pregnancy test --- will be excluded from this study due to uncertainty of the effects of MRI and TMS on the fetus 9. Not right-handed based on self-report (pre-screening) or evaluation with a standard test 10. Not a native English speaker.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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University of Nebraska Medical Center
RECRUITINGOmaha, Nebraska, 68198, United States
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