About this trial
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.
Eligibility criteria
Qualifiers
Age 18 years or older
Diagnosis of Tourette Syndrome
Moderate Tic Severity at baseline
Disqualifiers
Presence of metallic objects or neurostimulators in the brain
Pregnancy
History of active seizures or epilepsy
Contraindications to receiving fMRI
Trial design
Treatments tested in this trial
- transcranial magnetic stimulation
Treatment groups
Sponsors and collaborators
West Virginia University
Lead sponsor
University of Florida
Collaborator
Tourette Association of America
Collaborator