Actively Recruiting

Phase Not Applicable
Age: 5Years - 17Years
All Genders
NCT05370391

Comprehensive Behavioral Intervention for Tics

Led by University of Miami · Updated on 2026-01-29

200

Participants Needed

1

Research Sites

229 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this protocol is to examine treatment outcomes of youth receiving the Comprehensive Behavioral Intervention for Tics (CBIT) and better understand the predictors, moderators, mediators and/or mechanisms of change for this intervention.

CONDITIONS

Official Title

Comprehensive Behavioral Intervention for Tics

Who Can Participate

Age: 5Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • A current diagnosis of a DSM-5 Tic disorder (e.g., Tourette's Disorder/syndrome, Persistent (Chronic) Motor or Vocal Tic Disorder, or Provisional Tic Disorder) or caregiver/youth report of clinically impairing tic symptoms
  • Ability for youth to speak/read English sufficiently
  • At least one parent/caregiver available to sign study consent forms, remain present during assessments, and fill out study questionnaires in English.
Not Eligible

You will not qualify if you...

  • A current diagnosis of psychosis, bipolar disorder, intellectual disability, acute suicidality, alcohol/substance dependence, or eating disorder
  • Youth currently receiving psychotherapy elsewhere and/or have previously received CBIT
  • Currently suicidal or who have engaged in suicidal behaviors within the past 6 months
  • Youth currently taking psychotropic medication for a co-morbid psychiatric illness will be included without a wash-out period (to not delay treatment).

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Miami

Coral Gables, Florida, United States, 33124

Actively Recruiting

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Research Team

D

Danielle Ibarra, Psy.D.

CONTACT

M

Madison Bigler, B.A.

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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