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NCT06825520 · ClinicalTrials.gov registry record · NA
Investigating Changes in Premonitory Urges During Habit Reversal Training for Tics
A NA study of Tourette Syndrome in Adolescence and Tics, sponsored by University of Utah.
- Recruiting
- Registry status
- NA
- Development phase
- 6
- Enrollment target
- 1
- Study location
NCT06825520 is a NA study of Tourette Syndrome in Adolescence and Tics that is actively recruiting participants, run by University of Utah. The registered enrollment target is 6 participants, below the 47-participant average among 5 other Tourette Syndrome in Adolescence trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06825520, a NA study of Tourette Syndrome in Adolescence and Tics, is actively recruiting participants, sponsored by University of Utah.
- RECRUITING
- Registry status
- NA
- Development phase
- 6 participants
- Enrollment target
- 1
- Study location
Study Summary
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
Conditions Studied
Interventions
- BEHAVIORAL Habit Reversal Training
Study Locations (1)
Utah
- University of Utah - Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 6 participants |
| Start Date | 2025-02-11 |
| Est. Completion | 2026-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06825520
The ClinicalTrials.gov registry entry for NCT06825520 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 6 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 47-participant average among 5 other Tourette Syndrome in Adolescence trials with a reported enrollment target (87% lower). The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Tourette Syndrome in Adolescence appearing as the primary indexed condition, and to 1 intervention - of which Habit Reversal Training is the first listed.
NCT06825520 reports 1 study location spanning 1 distinct geographic area - top geographies include Utah.
Frequently Asked Questions
What is clinical trial NCT06825520 about?
NCT06825520 is a clinical study titled "Investigating Changes in Premonitory Urges During Habit Reversal Training for Tics". 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 ...
What is the current status of trial NCT06825520?
This trial is currently recruiting. It is a NA study. The enrollment target is 6 participants. The study started on 2025-02-11. Estimated completion is 2026-05.
What conditions does trial NCT06825520 study?
This clinical trial studies the following conditions: Tourette Syndrome in Adolescence, Tics, Tourette Syndrome in Children, Tourette Disorder.
What interventions are being tested in trial NCT06825520?
The interventions under investigation include: Habit Reversal Training (BEHAVIORAL).
Who is sponsoring clinical trial NCT06825520?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06825520 being conducted?
This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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