RECRUITING

Sensory Symptoms in Tourette Syndrome

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Patients with tics will be asked to complete a series of validated questionnaires (in electronic and/or paper format) regarding symptoms and conditions often associated with Tourette syndrome, including premonitory urges, sensory experiences, inattention, obsessive-compulsive tendencies, anxiety, and depression. Participants will also be asked to complete a quality of life assessment. This series of questionnaires will be administered annually.

Official Title

Sensory Symptoms in Tourette Syndrome

Quick Facts

Study Start:2019-04-17
Study Completion:2028-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03851484

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 18 years of age or older
  2. * Ability to provide informed consent and answer self-report questionnaires independently in English
  3. * Diagnosis of Tourette syndrome (TS), chronic motor tic disorder, or chronic vocal tic disorder
  1. * History of psychotic disorder
  2. * History of significant neurologic disorder (e.g., stroke) other than TS or another chronic tic disorder

Contacts and Locations

Study Contact

Michelle Eckland, BS
CONTACT
615-875-7394
michelle.r.eckland.1@vumc.org

Principal Investigator

David A Isaacs, MD, MPH
PRINCIPAL_INVESTIGATOR
Vanderbilt University Medical Center

Study Locations (Sites)

Vanderbilt University Medical Center
Nashville, Tennessee, 37232-5400
United States
Vanderbilt University Medical Center
Nashville, Tennessee, 37232
United States

Collaborators and Investigators

Sponsor: Vanderbilt University Medical Center

  • David A Isaacs, MD, MPH, PRINCIPAL_INVESTIGATOR, Vanderbilt University Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-04-17
Study Completion Date2028-12-31

Study Record Updates

Study Start Date2019-04-17
Study Completion Date2028-12-31

Terms related to this study

Keywords Provided by Researchers

  • Tourette syndrome
  • premonitory urge
  • sensory dysregulation
  • hypersensitivity

Additional Relevant MeSH Terms

  • Tourette Syndrome