One session of high-frequency rTMS to help with severe arm weakness after stroke
Official title: Effects of a Single Session of High-Frequency Repetitive Transcranial Magnetic Stimulation on Cortical Mapping of the Upper Limb in Stroke Patients With Severe Upper Limb Impairment
Run by Fundació Sant Joan de Déu · NCT07787793 · Data updated 2026-11-12
This study tests whether a single high-frequency rTMS session on the affected arm can reveal more motor signals in the brain of stroke patients who have little or no hand movement.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 54 (estimated) |
| Sponsor | Fundació Sant Joan de Déu Academic / other |
| Locations | 1 site (Palma, Balearic Islands) |
| Status | Recruiting |
| Started | September 15, 2026 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | August 26, 2026 |
| Trial ID | NCT07787793 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with a first-ever stroke lasting more than 6 months who cannot voluntarily activate hand muscles (finger extension score of 1 or less).
✕Probably not a fit
Patients with extensive corticospinal damage or contraindications to TMS may not benefit from this single-session intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study uses navigated TMS to map cortical motor activity before and after a single session of 10 Hz rTMS (600 pulses) delivered to the affected motor cortex, compared with sham stimulation, in stroke patients with severe upper limb impairment. The primary aim is to see if the rTMS session increases the number of motor-evoked potential positive points in the cortical map. Participants undergo a cortical motor mapping assessment, receive either real or sham stimulation, and then have a post-intervention mapping to detect any changes. The study addresses the gap in evidence for rTMS effectiveness in patients who are ME- P negative and have minimal voluntary hand function, considering mechanisms like diaschisis and latent corticospinal activity.
Why it matters
Potential benefit: If successful, patients could have improved cortical responsiveness that may support future rehabilitation options.
How similar studies have gone: Prior rTMS studies suggest increased cortical excitability in some patients, but evidence in ME- P individuals is limited and this approach is exploratory.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * First-ever stroke confirmed by MRI or CT scan. * Inability to voluntarily activate the hand musculature: manual muscle testing score of 1 or less in finger extension. * Time since stroke onset greater than 6 months. Exclusion Criteria: * History of craniotomy or metallic implants in the skull. * Diagnosis of uncontrolled epilepsy. * Diagnosis of other neurological diseases (dementia, Parkinson's disease, neuropathies, multiple sclerosis, or similar conditions). * Low level of consciousness or significant cognitive impairment that prevents informed consent or study collaboration. * Diagnosis of rheumatic disease or presence of hand deformities. * Pregnancy.
Where it's running
-
Hospital Sant Joan de Déu Palma
Palma, Balearic Islands, Spain Recruiting
Study contacts
- Principal investigator: Ancor Rebassa Cabrera, PT, MSc — Hospital Sant Joan de Deu
- Study coordinator: Ancor Rebassa Cabrera, PT, MSc
- Email: ancor.rebassa@sjd.es
- Phone: +34 607832655
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.