Adult Tic Disorders Registry (RegisTICs)

August 27, 2025 updated by: Assistance Publique - Hôpitaux de Paris
The purpose of this study is to develop the adult tic disorders registry in order to characterize the relationship between tic severity and tic-related impairment in women compared to men with tic disorders.

Study Overview

Status

Recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

450

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Clermont-Ferrand, France, 63003
        • Recruiting
        • CHU clermont-ferrand
        • Contact:
        • Principal Investigator:
          • Isabelle JALENQUES, MD
      • Limoges, France, 87042
        • Recruiting
        • CHU Limoges
        • Principal Investigator:
          • Jean-Luc HOUETO, MD
        • Contact:
      • Marseille, France, 13003
        • Recruiting
        • CHU Marseille
        • Contact:
        • Principal Investigator:
          • Tatiana WITJAS, MD
      • Paris, France, 75013
        • Recruiting
        • Service de Neurologie, GH Pitié Salpêtrière
        • Contact:
      • Poitiers, France, 86000
        • Recruiting
        • CHU Poitiers
        • Contact:
        • Principal Investigator:
          • Solène ANSQUER, MD
      • Saint-Herblain, France, 44800
        • Recruiting
        • Chu Nantes
        • Contact:
        • Principal Investigator:
          • Philippe DAMIER, MD
      • Strasbourg, France, 67200
        • Recruiting
        • CHU Strasbourg
        • Principal Investigator:
          • Mathieu ANHEIM, MD
        • Contact:

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.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patient with tics disorders

Description

Inclusion criteria :

  1. Age >18 years
  2. Patients with Tic disorders
  3. Given the non-opposition

Non Inclusion criteria

  1. No affiliation to a French health social insurance
  2. Significant congenital disorders that may affect understanding of assessments
  3. Patients under guardianship or curatorship

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Quality of life questionnaires
The scales (PUTS, OCI, TS-QOL, ASRS, GAD-7, PHQ9, TAPS) to be completed by the participant

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Correlation between Quality of Life and TICs severity
Time Frame: 6 months
Severity of the tics measurement (YGTSS Impairment Score) and the quality of life (TS-QOL) between men and women with tic disorders, while controlling for the YGTSS Total Tic Score
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in TICs
Time Frame: 6 months
Change in tic inventories/tic migrations with the YGTSS tic inventories
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 Major Dates

Study Start (Actual)

December 1, 2021

Primary Completion (Estimated)

December 1, 2027

Study Completion (Estimated)

December 1, 2027

Study Registration Dates

First Submitted

September 22, 2021

First Submitted That Met QC Criteria

October 11, 2021

First Posted (Actual)

October 25, 2021

Study Record Updates

Last Update Posted (Estimated)

September 4, 2025

Last Update Submitted That Met QC Criteria

August 27, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Tic Disorders

Clinical Trials on QOL to be completed by the participant

Subscribe