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Clinical Trials/NCT02413216
NCT02413216
Completed
Not Applicable

Creating a Computerized Self-administered Version of Comprehensive Behavioral Intervention for Tics

University of Utah2 sites in 1 country55 target enrollmentAugust 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tourette's Disorder
Sponsor
University of Utah
Enrollment
55
Locations
2
Primary Endpoint
Change in the Total Tic Severity Score on the Yale Global Tic Severity Scale (YGTSS)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Tic Disorders (including Tourette Disorder) are relatively common in school-age children and for some children can lead to significant psychosocial and physical impairment and diminished quality of life. Non-pharmacological treatments have been shown to be effective for reducing tics in some children. These treatment options are desired by parents, but are not widely available. The investigators recently developed an online, computerized, self-administered version of CBIT called TicHelper.com. The current study will test the efficacy of TicHelper.com in a randomized clinical trial.

Detailed Description

Effective non-pharmacological treatment options such as comprehensive behavioral intervention for tics (CBIT) have been shown to be effective for reducing tics in some children with chronic tic disorders, including Tourette's disorder. Although effective, many parents and children do not have access to a provider trained in these therapies and practical barriers such as travel and high costs for ongoing therapy limit treatment dissemination and utilization.The investigators recently developed an online, computerized, self-administered version of CBIT called TicHelper.com. This program is an 8-week online program designed to teach children and families empirically-supported tic management skills. The current study will test the efficacy of TicHelper.com in a randomized clinical trial in which 64 children with Tourette's Disorder or a persistent (chronic) tic disorder will be randomly assigned to 8-weeks of TicHelper.com (N=32) or an 8-week internet resource control condition (N=32). Tic symptoms will be assessed by a condition-blind independent evaluator at baseline, post-treatment, and 1-month follow-up. Information regarding patient acceptability of the program will also be collected. This project will test whether TicHelper.com is an efficacious and acceptable way to teach tic-management skills for children with tics.

Registry
clinicaltrials.gov
Start Date
August 2015
End Date
August 31, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mike Himle

Associate Professor

University of Utah

Eligibility Criteria

Inclusion Criteria

  • Child and parent are English speaking.
  • Child meets diagnostic criteria for Tourette's disorder or persistent (chronic) motor or vocal tic disorder according to the criteria of the Diagnostic and Statistical Manual of Mental Disorders - 5th Edition.
  • Child scores \>70 on a brief intelligence test
  • Child currently engages in at least one motor and/or vocal tic multiple times per day
  • Clinician rated tic severity score of \> 3 (mildly ill or worse)
  • Child is unmedicated for tics or associated conditions or has been on stable psychotropic medication for at least 6 weeks with no changes or planned changes in dosage.
  • Family has daily access to a personal computer with internet access and software meeting TicHelper minimum system requirements.

Exclusion Criteria

  • A Yale-Global Tic Severity Scale (YGTSS) score \> 30
  • Child scores \< 70 on intelligence test
  • Child meets diagnostic criteria for substance abuse or dependence or conduct disorder (within past 3 months) according to the criteria of the Diagnostic and Statistical Manual of Mental Disorders - 5th Edition.
  • Current or past non-drug treatment for tics that consisted of 4 or more sessions of habit reversal training or CBIT.
  • Child has lifetime diagnosis of mania or psychotic disorder
  • Child has any serious psychiatric or neurological condition not currently being managed, managed ineffectively, or requiring more immediate treatment other than that provided by the study.

Outcomes

Primary Outcomes

Change in the Total Tic Severity Score on the Yale Global Tic Severity Scale (YGTSS)

Time Frame: Baseline, Week 8 (post-treatment), Week 12 (1-month follow-up)

Clinician interview to assess overall severity of tics

Secondary Outcomes

  • Change in overall tic severity on the Clinician Global Impressions-Severity Scale(Baseline, Week 8 (post-treatment), Week 12 (1-month follow-up))
  • Clinician Global Impressions-Improvement Scale(Week 8 (post-treatment))
  • Clinician Global Impressions- Improvement Scale(Week 12 (1-month follow-up))

Study Sites (2)

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