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Adult Tic Disorders Registry

Adult Tic Disorders Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05090943
Acronym
RegisTICs
Enrollment
450
Registered
2021-10-25
Start date
2021-12-01
Completion date
2027-12-01
Last updated
2025-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tic Disorders

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.

Interventions

OTHERQOL to be completed by the participant

The scales (PUTS, OCI, TS-QOL, ASRS, GAD-7, PHQ9, TAPS) to be completed by the participant

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Correlation between Quality of Life and TICs severity6 monthsSeverity 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

MeasureTime frameDescription
Change in TICs6 monthsChange in tic inventories/tic migrations with the YGTSS tic inventories

Countries

France

Contacts

Primary ContactEmmanuel Flamand-Roze, MD, PhD
emmanuel.flamand-roze@aphp.fr1 42 16 06 45

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026