Investigating Changes in Premonitory Urges During Habit Reversal Training for Tics
Investigating Changes in Premonitory Urges During Habit Reversal Training
Who can join
Ages 8 to 17 · All sexes
Full 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 experiencing a PU for each of their target tics with a minimum rating of a 4/8 on a subjective rating (i.e., the Urge Thermometer; Silverman \& Albano, 1996) for each tic, 3. the targeted tics occur, on average, at least once per minute during a 10-minute direct observation, 4. are between the ages of 8 and 17 5. the patient has no planned changes in medication initiation or dosage during their study participation period. Exclusion Criteria: 1. the presence of any comorbid conditions that are considered a primary treatment concern and/or could interfere with study participation or treatment (i.e., unmanaged ADHD, OCD, anxiety), 2. have previously engaged in CBIT or HRT for more than 2 sessions, 3. a Yale Global Tic Severity Score of 40+ (or 20+ if they present with a primary motor or vocal tic disorder), 4. suspected (based on clinical presentation) that the tics are better attributed to functional neurological symptom disorder per DSM-5-TR criteria (APA, 2022).
About the study
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 separate tics, and a post assessment * Attend 5 practice sessions (approximately 30 minutes each) over a week for 3 weeks (total 15 practice sessions) * Study visits and practice sessions will take place in person and online via secure videoconference
What is being tested
- Habit Reversal Training (behavioral)
Sponsor: University of Utah · Participants: 6 · Started: Feb 11, 2025
Contact the study team
- Emily I Braley, MS · Phone: 801-585-7114
- Michael Himle, PhD · Phone: 801-581-7529
Official record on ClinicalTrials.gov — NCT06825520
Locations in the U.S.
| Utah | University of Utah, Salt Lake City |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.