Zapping the brain to rewire stroke-damaged hands?
NCT ID NCT06809959
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a gentle, non-invasive brain stimulation technique called tACS could improve hand function in 20 stroke survivors. The stimulation targeted two key brain areas involved in movement planning. Researchers measured brain connectivity and hand movement patterns to see if the stimulation helped. The study was small and focused on measuring brain changes, not yet on proving a treatment works.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcranial alternating current stimulation (tACS) device
- What this could lead to
- If it works, this could point toward a non-invasive way to improve hand and arm recovery after stroke.
- What could go wrong
- This was a very small, early study (20 people) that looked at brain signals, not actual function. Results may not lead to a proven treatment.
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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20 people
The number who actually took part.
- Started
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Feb 2025
- Finished
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Apr 2026
- 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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18 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * First-ever clinical stroke * Signed informed consent * First-ever clinical ischemic stroke at least 3 months ago * Stimulation areas (PMv and IPS) are unaffected * Residual deficits in the upper limb Exclusion Criteria: * Presence of additional neurological or psychiatric disorders * Use of psychotropic medication * Pregnancy or potential pregnancy in female participants * Pacemakers, other stimulators, or medication pumps * Claustrophobia * Non-MRI-compatible metallic implants or foreign objects in the body * Contraindications for transcranial alternating current stimulation (e.g., epilepsy, history of seizures, any type of pacemaker)
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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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Department of Neurology, University Medical Center Hamburg-Eppendorf
Hamburg, 20246, Germany
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