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Clinical Trials/NCT05090943
NCT05090943RecruitingNot Applicable

Adult Tic Disorders Registry

Assistance Publique - Hôpitaux de Paris7 sites in 1 country150 target enrollmentStarted: December 1, 2021Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
150
Locations
7
Primary Endpoint
Correlation between Quality of Life and TICs severity
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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 Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

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

Secondary Outcomes

  • Change in TICs(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (7)

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