Trichotillomania Clinical Trial
— CBT for TTMOfficial title:
Cognitive Behavioral Therapy for Trichotillomania
Verified date | June 2012 |
Source | Massachusetts General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
This study aims to develop a comprehensive Cognitive Behavioral Therapy protocol for adult patients with Trichotillomania that emphasizes relapse prevention and that addresses comorbid affective symptoms, as well. The study will compare the efficacy of CBT with a minimal attention control (MAC)condition. We hypothesize that outcome at post-treatment, 3-month, and 6-month follow-up will be better for the CBT vs. MAC condition including higher responder rates and greater reduction in hair pulling severity.
Status | Completed |
Enrollment | 38 |
Est. completion date | January 2012 |
Est. primary completion date | January 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - primary DSM-IV diagnosis of TTM - outpatients who are 18 or older - a minimum MGHHPS total scale score of 10 - a minimum TTM symptom duration of 1 year with no significant remissions (as defined by complete abstinence of hair extraction for a 2-week period during the prior 6 months) Exclusion Criteria: - presence of a serious psychiatric condition including mental retardation, psychosis, pervasive developmental disorder, organic mental disorders, manic episode, ADHD, suicidality, lifetime alcohol or substance dependence, or alcohol or substance abuse within the past 3 months - presence of a serious medical condition that would limit ability to routinely attend sessions and complete homework assignments - individual or group psychotherapy (not addressing TTM) that has not been ongoing for the past 3 months and/or without intent to continue same treatment during study tenure) - previous CBT for TTM - involvement in other treatment for TTM - psychotropic medication that has not been stable for 3 months prior to study enrollment and/or without intent to continue same medication regimen during study tenure) |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Massachusetts General Hospital | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Massachusetts General Hospital | Emory University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Massachusetts General Hospital Hair Pulling Scale (MGHHPS) | Baseline, weekly visits, follow-up | No | |
Primary | NIMH Trichotillomania Severity Scale (NIMH-TSS) | Baseline, weekly visits, follow-up | No | |
Primary | NIMH Trichotillomania Impairment Scale (NIMH-TIS) | Baseline, weekly visits, follow-up | No |
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