Actively Recruiting

Phase Not Applicable
Age: 6Years - 21Years
All Genders
Healthy Volunteers
ID07325175

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

Led by Children's Hospital Medical Center, Cincinnati · Updated on 2026-01-08

75

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to understand how childhood dystonia, a movement disorder, develops and progresses in children. It focuses on how the brain's motor networks change during motor development and how deep brain stimulation (DBS) affects these networks in children with dystonia. The study will explore neural activity both at rest and during simple motor tasks to gain insights into motor function changes over time. Participants will have noninvasive measurements like EEG and EMG to record brain and muscle activity. Children with DBS will be evaluated both when the device is active and inactive to see how stimulation influences motor network function. This study involves repeated assessments over about two years to track changes in brain activity and connectivity. During the study, participants will undergo neurophysiological tests at different times, including resting and task conditions. The research team will measure changes in motor network activity and brain connectivity using EEG data. Safety and ability to complete the study tasks will be monitored, and the primary outcome is the change in motor network aperiodic activity over time. The total duration includes baseline and follow-up assessments spanning an average of two years.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 6Years - 21Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of dystonia (with or without DBS) for dystonia subjects
  • Willingness and ability to complete study protocols
  • Normal developmental milestones for typically developing controls
  • No neuropsychiatric disorders for typically developing controls
  • No significant medical conditions for typically developing controls
  • Age between 6 and 21 years
Not Eligible

You will not qualify if you...

  • History of epilepsy
  • Presence of implanted medical devices except DBS in dystonia subjects
  • Lack of cognitive or physical ability to complete study protocol

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - Baseline and through study completion, an average of 2 years

Participants with DBS undergo neurophysiological recordings with DBS on and off to assess motor network dynamics.

Multiple visits over 2 years for recordings with DBS on and off

Trial Site Locations

Total: 1 location

1

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, United States, 45229

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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