Investigating Changes in Premonitory Urges During Habit Reversal Training for Tics
A legfontosabb adatok
- Hol
- Salt Lake City (Egyesült Államok)A helyszín megnézése
Neked szólhat?
Magadról válaszolj. Ez nem döntés: hogy részt vehetsz-e, azt csak a vizsgálat csapata mondhatja meg.
- 8 és 17 év között vagy?
Forrás: NCT06825520: ki vehet részt
Helyszínek itt: Egyesült Államok
- University of UtahSalt Lake City, Egyesült ÁllamokContact: Emily I Braley, MSRésztvevőt keres
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- University of Utah
- Azonosító
- NCT06825520
- A regiszteradat frissítve
- 2025. május 28.
- Eredeti leírás
The primary aim of this study is to learn more about premonitory urges (PU) when using Habit Reversal Training (HRT) to treat tics.A teljes eredeti leírásKevesebb
Investigating Changes in Premonitory Urges During Habit Reversal Training
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
Bevonási feltételek: 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; present with at least three motor and/or vocal tics and are interested in receiving treatment,; 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,; the targeted tics occur, on average, at least once per minute during a 10-minute direct observation,; are between the ages of 8 and 17; the patient has no planned changes in medication initiation or dosage during their study participation period.
Kizáró feltételek: have previously engaged in CBIT or HRT for more than 2 sessions,; 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),; a Yale Global Tic Severity Score of 40+ (or 20+ if they present with a primary motor or vocal tic disorder),; suspected (based on clinical presentation) that the tics are better attributed to functional neurological symptom disorder per DSM-5-TR criteria (APA, 2022).