Epidemiology of Assertiveness and Emotion Management Disorders in People With Tourette's Syndrome
AFFIRMATICS
1 other identifier
interventional
350
1 country
1
Brief Summary
The goal of this study is to evaluate the proportion of assertiveness difficulties in Tourette syndrome. Participants will complete several e-questionnaires (on assertiveness, Tourette severity, quality of life, self-esteem and comorbidities like depression, anxiety...).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started May 2024
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 13, 2023
CompletedFirst Posted
Study publicly available on registry
November 18, 2023
CompletedStudy Start
First participant enrolled
May 6, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 5, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
November 5, 2026
ExpectedFebruary 27, 2026
February 1, 2026
2 years
November 13, 2023
February 25, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Rathus assertiveness questionnaire
The Rathus assertiveness questionnaire includes 30 items, each scores from -3 to +30. A total score inferior or equal to -9 reveals assertiveness difficulties.
5 minutes at inclusion
Secondary Outcomes (6)
MOVES
less than 5 minutes at inclusion
HADS
3 minutes at inclusion
ASRS-5
2 minutes at inclusion
Rosenberg Self-Esteem Scale
2-3 minutes at inclusion
DERS
5 minutes at inclusion
- +1 more secondary outcomes
Study Arms (1)
Rathus Assertiveness scale
EXPERIMENTALAll participants
Interventions
Eligibility Criteria
You may qualify if:
- Tourette syndrome
- Participants aged 18 years or over
You may not qualify if:
- Participants under legal protection
- Inability to complete questionnaires alone
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Clermont-Ferrand
Clermont-Ferrand, France, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Isabelle JALENQUES
University Hospital, Clermont-Ferrand
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 13, 2023
First Posted
November 18, 2023
Study Start
May 6, 2024
Primary Completion
May 5, 2026
Study Completion (Estimated)
November 5, 2026
Last Updated
February 27, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share