Registry for adults with tic disorders

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to create a registry for adults with tic disorders to better understand the relationship between tic severity and the resulting impairment in both women and men. Participants will complete quality of life assessments to provide valuable data for analysis. The study focuses on characterizing differences in tic disorders based on gender, which may lead to improved understanding and management of these conditions.

Why it matters

Who can join: the full rules

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

Where it's running

• CHU Clermont-Ferrand
  Clermont-Ferrand, France Recruiting
• CHU Limoges
  Limoges, France Recruiting
• CHU Marseille
  Marseille, France Recruiting
• Service de Neurologie, GH Pitié Salpêtrière
  Paris, France Recruiting
• CHU Poitiers
  Poitiers, France Recruiting
• CHU Nantes
  Saint-Herblain, France Recruiting

Study contacts

• Study coordinator: Emmanuel Flamand-Roze, MD, PhD
• Email: emmanuel.flamand-roze@aphp.fr
• Phone: 1 42 16 06 45

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Mindfulness intervention for managing tics in Tourette syndrome

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• Comparing Sertraline and Placebo for Treating Anxiety in Children with Neurodevelopmental Disorders

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• Characterizing Repetitive Behaviors in OCD and Tic Disorders

  This study is testing if special brain activity measurements can help tell the difference between compulsions in OCD and tics in Tourette syndrome to improve treatment options for people aged 15 to 65.

  Recruiting at 3 sites Institut National de la Santé Et de la Recherche Médicale, France · Créteil and 2 other locations · NCT06050369

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.