Can brain stimulation help stroke survivors relearn movement?
NCT ID NCT07834333
First seen Sep 22, 2026 · Last updated Sep 23, 2026 · Updated 1 time
Summary
Researchers are testing whether theta burst stimulation, a noninvasive form of brain stimulation, can improve arm and leg recovery when added to standard rehabilitation after a first ischemic stroke. The trial enrolls 60 adults aged 45 and older who are within three months of their stroke. Participants receive either active stimulation over the motor cortex, sham stimulation, or a combination, alongside at least four weeks of conventional therapy. The main measure is change in upper-extremity movement, with follow-up one month after treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- theta burst stimulation, a form of noninvasive brain stimulation
- What this could lead to
- If it works, this could point toward a way to boost standard rehabilitation and help stroke survivors regain more arm and leg movement.
- What could go wrong
- The trial is small, with 60 people at one hospital, and brain stimulation has produced mixed results in stroke recovery. Benefits may be modest or fade, and the procedure can cause scalp discomfort or headaches.
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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.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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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45 years and older
- 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: * Diagnosis of ischemic stroke due to middle cerebral artery (MCA) occlusion confirmed by magnetic resonance imaging (MRI). * Within the first 3 months after stroke. * First-ever stroke. * Age ≥45 years. * Brunnstrom stage 1, 2, or 3 for the upper extremity and hand. * No previous physical therapy after the current stroke. * Ability to maintain at least minimal semi-sitting balance. * Medically and neurologically stable. * Mini-Mental State Examination score \>24. * Native Turkish speaker who voluntarily agrees to participate and provides written informed consent. Exclusion Criteria: * History of epilepsy. * Presence of a pacemaker. * Pregnancy. * Neurological disease other than stroke. * Metallic implants in the brain or scalp, including cochlear implants. * History of brain surgery. * Comorbid disease that may significantly impair general health, such as heart f-failure or chronic obstructive pulmonary disease, and/or severe infection. * Diagnosis of malignancy. * Peripheral nerve injury and/or musculoskeletal disorder affecting motor function of the upper or lower extremities, such as fracture. * Cardiac arrhythmia. * Aphasia, spatial neglect, or visual field loss. * Visual or hearing impairment that prevents communication. * Alcohol and/or drug dependence. * Refusal to participate or failure to provide informed consent.
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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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Ankara Etlik Şehir Hastanesi
RECRUITINGAnkara, Yenimahalle, 06170, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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