Clinical trial Recruiting at 1 site Interventional Ages 18 to 80

See if repetitive transcranial magnetic stimulation helps with dystonia symptoms

Official title: The Effect of Repetitive Trans-cranial Magnetic (rTMS) Stimulation on Abnormal Cortical Hubs Identified by Functional Magnetic Resonance in Subjects With Dystonia

Run by Northwell Health · NCT07626216 · Data updated 2026-11-12

This study tests whether applying rTMS can alter brain activity to help people with dystonia.

More Dystonia Disorder trials

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment10 (estimated)
SponsorNorthwell Health
Academic / other
Drugs / interventionsradiation
Locations1 site (Manhasset, New York)
StatusRecruiting
StartedMarch 4, 2026
Main results expectedMay 2028
Study endsMay 2029
Registry record updatedNovember 6, 2026
Trial IDNCT07626216 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18-80 with focal, segmental, or generalized dystonia (including DYT1 or DYT6) and a normal neurological exam aside from dystonia.

Probably not a fit

Patients with unrelated dystonia types (e.g., heredodegenerative forms beyond DYT1/DTY6 criteria) or significant comorbidities may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot study uses resting-state fMRI to identify brain network targets and then applies repetitive transcranial magnetic stimulation to see if targeted stimulation can modulate abnormal brain connectivity in dystonia. The approach combines imaging analysis with non-invasive brain stimulation to explore potential symptom improvement. Eligibility includes adults with dystonia that is focal, segmental, or generalized and related to DYT1 or DYT6 dystonia, while excluding other neurodegenerative or systemic conditions. The study is conducted at Northwell Health's Feinstein Institutes, with a single intervention modality using rTMS.

Why it matters

Potential benefit: If successful, patients could experience improved motor control and reduced dystonia-related symptoms through non-invasive therapy.

How similar studies have gone: Previous neuroscience work suggests non-invasive brain stimulation can modulate dystonia networks, but direct rTMS targeting based on resting-state fMRI is an emerging, exploratory approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Male or female
* 18 and 80 years of age.
* Patients who manifest dystonia - sustained involuntary movement of the head, neck, trunk or limbs.
* The dystonia may be spontaneous or genetic, specifically DYT1 or DYT6 and then only those patients who are demonstrating dystonia. The patient/subject will have a normal neurological exam except for dystonia.

Exclusion Criteria:

* Heredodegenerative dystonia of the type DYT8,9 or 10.
* Past history of head trauma, stroke, epilepsy, demyelinating disease
* Hypertension in excess of 160mmHg systolic and 90mmHg diastolic
* Congestive heart failure
* Diabetes
* Past psychiatric conditions: e.g., depression
* Systemic metabolic disease: e.g., Wilson's disease, progressive neurodegenerative disease (like supranuclear palsy or corticobasal ganglionic degeneration)
* Magnetizable incorporated metal parts - like pacemakers
* History or diagnosis of Parkinson's disease
* Presence of myoclonus
* No previous surgery for dystonia
* Long term exposure to benzodiazepines, neuroleptics or anticonvulsants
* No botulinum toxin within 12 weeks of baseline assessment and fMRI.
* Moderate to severe cognitive impairment (judged by a minimental status of \<24.)

Where it's running

  • Northwell Health/Feinstein Institutes
    Manhasset, New York, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.