Adult Tic Disorders Registry
ConditionTic Disorders
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age >18 years
Patients with Tic disorders
Given the non-opposition
No affiliation to a French health social insurance
Disqualifiers
None
Trial population
Patient with tics disorders
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
QOL to be completed by the participant
Other interventionThe scales (PUTS, OCI, TS-QOL, ASRS, GAD-7, PHQ9, TAPS) to be completed by the participant
Treatment groups
450 Participants
are divided into 1 treatment groupGroup A: Quality of life questionnaires1 intervention
Trial outcomes
Primary outcomes
1
Correlation between Quality of Life and TICs severity
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
Time frame
6 monthsSecondary outcomes
1
Change in TICs
Change in tic inventories/tic migrations with the YGTSS tic inventories
Time frame
6 monthsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov