Actively Recruiting

Age: 18Years +
All Genders
NCT04851678

Longitudinal Impact of Stressors in Adults With Tourette Syndrome

Led by Vanderbilt University Medical Center · Updated on 2026-05-05

140

Participants Needed

1

Research Sites

299 weeks

Total Duration

On this page

Sponsors

V

Vanderbilt University Medical Center

Lead Sponsor

U

University of California, Los Angeles

Collaborating Sponsor

AI-Summary

What this Trial Is About

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).

CONDITIONS

Official Title

Longitudinal Impact of Stressors in Adults With Tourette Syndrome

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults over 18 years old meeting DSM-V criteria for Tourette syndrome, chronic motor tic disorder, or chronic vocal tic disorder
  • Ability to provide informed consent
  • Proficiency in English
Not Eligible

You will not qualify if you...

  • Significant medical, neurological, or psychiatric diagnoses other than Tourette syndrome and its commonly co-occurring psychiatric conditions (e.g., uncontrolled epilepsy, chronic heart failure, schizophrenia)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Vanderbilt University Medical Center

Nashville, Tennessee, United States, 37232-5400

Actively Recruiting

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Research Team

M

Michelle Eckland, BS

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Longitudinal Impact of Stressors in Adults With Tourette Syndrome | DecenTrialz