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Clinical Trials/NCT03628703
NCT03628703CompletedNot Applicable

Using Repetitive Transcranial Magnetic Stimulation to Modulate Response Inhibition in Tourette Syndrome

Children's Hospital Medical Center, Cincinnati1 site in 1 country10 target enrollmentStarted: April 22, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
10
Locations
1
Primary Endpoint
Stop Signal Reaction Time (SSRT)

Study Overview

Brief Summary

Tics are the hallmark symptoms in Tourette Syndrome. Patients with Tourette Syndrome have difficulties controlling unwanted movements. The ability to control the motor system involves the pre-supplementary motor area (pre-SMA) in the brain. In this study, we will use Transcranial Magnetic Stimulation to modulate the pre-SMA and determine effect on the ability to stop an unwanted action in a behavior task (stop signal task).

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
10 Years to 17 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Tourette Syndrome

Exclusion Criteria

  • •Autism spectrum disorder
  • •Mood disorder
  • •Implanted medical device (e.g. pacemaker, shunt, pumps)

Arms & Interventions

Repetitive TMS

Experimental

Repetitive Intermittent Theta-Burst Transcranial Magnetic Stimulation

Intervention: Repetitive TMS (Device)

Outcomes

Primary Outcomes

Stop Signal Reaction Time (SSRT)

Time Frame: 30 minutes after Repetitive Transcranial Magnetic Stimulation (as it takes about 30 minutes to complete the modified Slater-Hammel stop signal task)

SSRT measured from modified Slater-Hammel stop signal task performance. The SSRT is calculated by subtracting the average stop signal delay (msec) from the average go-trial reaction time. The SSRT is a measure of inhibitory behavior. The lower the SSRT value means a person is better at inhibitory control. The higher the SSRT value means a person is worse at inhibitory control.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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