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.
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