Clinical trial Recruiting at 1 site Interventional Ages 6 to 21

Measuring brain network activity to predict and improve outcomes in children with dystonia

Official title: Quantifying Motor Network Dynamics to Predict and Enhance Outcomes in Pediatric Dystonia

Run by Children's Hospital Medical Center, Cincinnati · NCT07325175 · Data updated 2026-11-12

This project will test whether noninvasive brain and muscle recordings, and comparing DBS on versus off, can predict and help improve motor outcomes for children with dystonia.

Quick facts

Study typeInterventional
Ages6 Years to 21 Years
SexAll
Enrollment75 (estimated)
SponsorChildren's Hospital Medical Center, Cincinnati
Academic / other
Locations1 site (Cincinnati, Ohio)
StatusRecruiting
StartedSeptember 1, 2026
Main results expectedAugust 31, 2031
Study endsAugust 31, 2031
Registry record updatedOctober 20, 2026
Trial IDNCT07325175 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are children diagnosed with dystonia (with or without an implanted DBS system) who can follow simple instructions and tolerate EEG/EMG testing, while typically developing children without neuropsychiatric conditions may join as controls.

Probably not a fit

Children with a history of epilepsy, other implanted medical devices (except DBS in dystonia subjects), or those unable to complete the testing due to severe cognitive or physical limitations are unlikely to benefit from participation.

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

What this trial studies

The study uses EEG and EMG recordings at rest and during a simple motor reaction task to map cortical and subcortical motor network activity in children with dystonia. Children who have deep brain stimulation will be tested with the device both on and off to measure effects of chronic and active stimulation on network function. Data from dystonia participants will be compared to typically developing controls to track how motor networks evolve with development. Researchers aim to identify neural patterns that predict response to DBS and could guide individualized stimulation settings.

Why it matters

Potential benefit: If successful, this approach could help doctors personalize DBS settings and predict which children are most likely to benefit, improving motor function and quality of life.

How similar studies have gone: Prior adult studies have shown that DBS changes motor network activity measurable with EEG/EMG, but applying these quantitative network measures in pediatric dystonia is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* For dystonia subjects:
* Dx of dystonia (with and without DBS)
* willingness and ability to complete study protocols.
* For Typically Developing Controls:
* normal developmental milestones
* absence of any neuropsychiatric disorder
* no significant medical condition.

Exclusion Criteria:

* history of epilepsy
* presence of implanted medical devices (except DBS in dystonia subjects)
* lack of cognitive or physical ability to complete study protocol.

Where it's running

  • Cincinnati Children's Hospital Medical Center
    Cincinnati, Ohio, United States
    Recruiting

Similar studies

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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.