Investigating Changes in Premonitory Urges During Habit Reversal Training for Tics

Recruiting N/A Interventional Study
Tics Tourette Disorder Tourette Syndrome in Children Tourette Syndrome in Adolescence
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
8 – 17
Sex
Any
Study type
Interventional
Purpose
Basic Science
Participants needed
6 (estimated)
Sponsor
University of Utah · Other
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About This Trial
The primary aim of this study is to learn more about premonitory urges (PU) when using Habit Reversal Training (HRT) to treat tics. The main focus of this study is to investigate if and when PU change during tic treatment sessions and between tic treatment sessions. Participants will: * Attend 5 study visits (approximately 1 to 1.5 hours each) for an intake, habit reversal training for 3 separa…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: Participants who meet criteria for a DSM-5-TR diagnosis of a TD will be recruited to participate in this study. Participants will be eligible for the study if they 1. present with at least three motor and/or vocal tics and are interested in receiving treatment, 2. report experi…
Contacts

Emily I Braley, MS

801-585-7114

theticlab@utah.edu

CONTACT

Michael Himle, PhD

801-581-7529

michael.himle@utah.edu

CONTACT