Actively Recruiting

Phase Not Applicable
Age: 12Years - 21Years
All Genders
NCT06270251

Modeling Tic Change During Behavior Therapy for Tics

Led by University of Minnesota · Updated on 2026-03-19

30

Participants Needed

1

Research Sites

235 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic tics are a disabling neuropsychiatric symptom associated with multiple child-onset mental disorders. Chronic tics affect 1-3% of youth and can be associated with impaired functioning, emotional and behavioral problems, physical pain, diminished quality of life, and peer victimization. Chronic tics are the primary symptom of Tourette Syndrome (TS) and Persistent Motor/Vocal Tic Disorders. CBIT is a manualized treatment focused on increasing tic controllability. Its core procedure is competing response training (CRT), in which patients learn to inhibit tics by learning and applying a competing motor action to one tic at a time. CBIT is recommended as a first-line treatment relative to medications and other therapies. However, only 52% of children and 38% of adults show clinically meaningful tic improvement. Large randomized trials have demonstrated the superiority of CBIT over supportive therapy in child and adult patients, and meta-analysis shows comparable effect sizes for CBIT and medication. Although increasing tic controllability is the primary goal of CBIT, tic controllability nor its correlates have been examined longitudinally during the intervention. The overall objective of this study is to use fine-grained data collection strategies to identify patterns in tic controllability and other relevant related variables that are associated with treatment response to CBIT. Participants with chronic tics will complete a manualized course of 8-session CBIT. Behavioral, psychosocial, and global functioning will be assessed longitudinally to examine predictors and correlates of response. CBIT sessions will be video recorded.

CONDITIONS

Official Title

Modeling Tic Change During Behavior Therapy for Tics

Who Can Participate

Age: 12Years - 21Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 12-21 years at time of enrollment
  • Current chronic motor and/or vocal tics for at least 1 year without a tic-free period longer than 3 consecutive months
  • Tics not caused by a medical condition or substance effects
  • Moderate or greater tic severity (Yale Global Tic Severity Scale total score 14; or 9 for motor or vocal tics only)
  • Full scale IQ greater than 70
  • Fluent in English to understand study measures and instructions
Not Eligible

You will not qualify if you...

  • Active suicidality
  • Previous diagnosis of psychosis or cognitive disability
  • Substance abuse or dependence within the past year
  • Concurrent psychotherapy focused on tics
  • Use of neuroleptic or antipsychotic medications
  • Taking medication not stable for at least 6 weeks with no planned dose changes

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Minnesota

Minneapolis, Minnesota, United States, 55414

Actively Recruiting

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Research Team

B

Brianna Wellen, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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