Thinking of joining a study?

Register your interest

NCT05705999 | Recruiting | Tourette Syndrome


Strengthening Tourette Treatment OPtions Using TMS to Improve CBIT, a Double-blind, Randomized, Controlled Study
Sponsor:

West Virginia University

Information provided by (Responsible Party):

Jessica Frey

Brief Summary:

This pilot study will investigate the clinical and neurophysiological effects of repetitive transcranial magnetic stimulation (rTMS) followed by comprehensive behavioral intervention for tics (CBIT) in adult patients with Tourette's Syndrome (TS). Two groups of moderate disease severity will be randomized to receive active or sham rTMS targeted to the supplementary motor area (SMA) followed by eight CBIT sessions. The change in tic frequency and severity (primary outcome) and neurophysiological changes (secondary outcome) will be compared between the two groups. The central hypothesis is that low frequency rTMS will augment the effects of CBIT through favorable priming of the SMA network.

Condition or disease

Tourette Syndrome

Intervention/treatment

transcranial magnetic stimulation

Phase

Not Applicable

Study Type : Interventional
Estimated Enrollment : 20 participants
Masking : Double
Primary Purpose : Treatment
Official Title : Strengthening Tourette Treatment OPtions Using TMS to Improve CBIT, a Double-blind, Randomized, Controlled Study
Actual Study Start Date : March 12, 2024
Estimated Primary Completion Date : March 30, 2025
Estimated Study Completion Date : December 30, 2025
Arm Intervention/treatment

Active Comparator: Active rTMS

Patients receiving active rTMS

Device: transcranial magnetic stimulation

Sham Comparator: Sham rTMS

Patients receiving sham rTMS

Device: transcranial magnetic stimulation

Ages Eligible for Study: 18 Years to 100 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
Criteria
Inclusion Criteria
  • Age 18 years or older
  • Diagnosis of Tourette Syndrome
  • Moderate Tic Severity at baseline
Exclusion Criteria
  • Presence of metallic objects or neurostimulators in the brain
  • Pregnancy
  • History of active seizures or epilepsy
  • Contraindications to receiving fMRI
  • Inability to participate in CBIT due to other underlying cognitive or medical condition

Strengthening Tourette Treatment OPtions Using TMS to Improve CBIT, a Double-blind, Randomized, Controlled Study

Location Details


Please Choose a site



Strengthening Tourette Treatment OPtions Using TMS to Improve CBIT, a Double-blind, Randomized, Controlled Study

How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations


Recruiting

United States, West Virginia

WVU RNI

Morgantown, West Virginia, United States, 26506

Loading...