Longitudinal Impact of Stressors in Adults With Tourette Syndrome

Recruiting Observational Study
Tourette Syndrome
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
140 (estimated)
Sponsor
Vanderbilt University Medical Center · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

The Investigators propose a two-year, longitudinal pilot study of TS adults (\>18) to determine impact of lifetime environmental stress exposure on tic severity, psychiatric comorbidity severity, and health-related quality of life (HRQOL).

Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * adults (\>18) meeting Diagnostic and Statistics Manual, 5th edition (DSM-V) criteria for Tourette syndrome, chronic motor tic disorder, or chronic vocal tic disorder * ability to provide informed consent * English proficiency Exclusion Criteria: \- significant medical, neuro…
Contacts

Michelle Eckland, BS

615-875-7394

michelle.r.eckland.1@vumc.org

CONTACT