NCT Number: NCT00218777
Cognitive Behavior Therapy and Habit Reversal Training for the Treatment of Chronic Tic Disorders in Children
This study will determine the effectiveness of cognitive behavior therapy (CBT) with habit reversal training (HRT) in treating chronic tic disorders (CTDs) in children and adolescents.
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Notify MeKey information
Conditions
Age range
9 year–17 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2 / Phase 3
Primary location
UCLA Child OCD, Anxiety, and Tic Disorders Program, Los Angeles, California, United States
About this study
CTDs and Tourette syndrome are neurobehavioral disorders that are characterized by a persistent pattern of motor and vocal tics. Tics are intermittent movements or sounds that occur repeatedly. They can be either brief, rapid, and darting movements or more purposeful movements, such as repetitively locking and unlocking a door. Vocal tics can be simple, as in sniffing or grunting, or more complex, such as complete words or phrases. Tic disorders can cause considerable distress in affected children, and can lead to social and academic impairment. If left untreated, CTDs can last into adulthood. The standard treatment for suppressing CTDs is medication; dopamine-blocking drugs are used most commonly. These medications, however, are associated with a range of adverse effects that can result in poor treatment compliance and premature treatment termination. Recent research suggests that HRT may be an effective, lower risk treatment for CTDs. HRT is a behavioral treatment based on increasing awareness of one's behaviors and replacing unwanted behaviors with less bothersome ones. This study will determine the effectiveness of CBT with HRT in treating CTDs in children and adolescents.
Participants in this double blind study will be randomly assigned to receive either CBT plus HRT or standard care, which will consist of psychoeducation and supportive therapy. All participants will partake in 8 sessions of their assigned therapy over the course of 10 weeks. After the initial 10 weeks, those who responded to treatment will report back to the study site for 3 monthly booster sessions. Changes in tic severity, effects of the therapies on overall functioning and quality of life, and possible predictors of treatment outcome will be assessed.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Meets DSM-IV diagnostic criteria for chronic tic disorder (chronic motor or vocal tic disorder or Tourette syndrome)
- Score of at least 3 on the Clinical Global Impressions Severity Scale
- Score of at least 14 on the Yale Global Tic Severity Scale (YGTSS) or at least 10 for individuals with motor tics only
- Unmedicated or currently on a stable medication treatment for tics, obsessive compulsive disorder (OCD), ADHD, anxiety, and/or depressive disorder for at least 6 weeks, with no planned changes for the duration of study participation
- Child speaks English
Exclusion criteria
- Score greater than 30 on the YGTSS
- IQ less than 80 on the Wechsler Abbreviated Scale of Intelligence (WASI)
- Meets DSM-IV criteria for substance abuse or dependence within the 3 months prior to study entry
- Meets DSM-IV criteria for conduct disorder within the 3 months prior to study entry
- Lifetime DSM-IV diagnosis of pervasive developmental disorder, mania, or psychotic disorder
- Any serious psychiatric, psychosocial, or neurological condition (i.e., OCD, ADHD, major depressive disorder, anxiety, severe aggression, or family discord) requiring immediate treatment other than what is provided in the current study (i.e., medication, school intervention, or family therapy)
- Previous treatment with four or more sessions of HRT for tics
Treatment and study plan
Primary outcomes
-
Reduction in tic severity
Time frame: 10-22 weeks
-
Reduction in tic-related impairment and distress (measured at Week 10)
Time frame: measured at week 10
Secondary outcomes
-
Tic severity and associated impairment and distress (measured at Week 36 follow-up)
Time frame: measured at week 36 follow-up
-
Changes in neurocognitive function (measured at Week 10)
Time frame: measured at week 10
Sponsors and collaborators
Lead sponsor
Tourette Association of America
Other
Collaborators
- National Institute of Mental Health (NIMH)
Registry information
Official study title
Behavior Therapy for Children With Chronic Tic Disorders
Acronym: CBIT
Important dates
- Study start
- 2004
- Primary completion
- 2007
- Study completion
- 2007
- First posted
- Sep 22, 2005
- Registry last updated
- Dec 14, 2015
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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