Treatment Study Investigating New Cognitive Behavioral Therapy Treatment Manual for Body Dysmorphic Disorder

StatusCompleted
PhaseNot applicable
Started

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Record History

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  1. Re-verified, no change to tracked fieldsv11
  2. Notable Lead sponsor: National Institute of Mental Health (NIMH) to Massachusetts General Hospital
    • Collaborators expanded, about 6 words
    v10
  3. Minor Trial status: Active, Not Recruiting to Completedv9
  4. Re-verified, no change to tracked fieldsv8
  5. Minor Primary completion date: Dec 2008
    • Study completion date: Feb 2008 to Dec 2008
    • Interventions: Cognitive behavioral therapy (Behavioral) to Cognitive behavioral therapy (CBT) (Behavioral)
    v7
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  1. Minor Trial status: Recruiting to Active, Not Recruitingv6 Show 4 more changesShow less
    • Study completion date: Feb 2007 to Feb 2008
    • Secondary endpoints: details revised at 3 of 3 entries
    • Site details revised at 2 of 2 sites
    • Study arms: 0 to 2
  2. Minor Site contacts updated at 1 of 2 sitesv5
  3. 2 versions Re-verified since Nov 18, 2005, no change to tracked fieldsv3-v4
  4. Minor Enrollment target: 48 to 36
    • Study description expanded, about 43 words
    • Study title expanded, about 1 word
    v2
  1. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
In an earlier phase of this study, a cognitive behavioral therapy (CBT) manual to treat body dysmorphic disorder (BDD) symptoms was developed. We are currently implementing this manual-based treatment to validate its effectiveness in patients with BDD.
Trial Details
NCT Number NCT00106223
Lead Sponsor Massachusetts General Hospital
Collaborators: National Institute of Mental Health (NIMH)
Conditions
(from sponsor)
Body Dysmorphic Disorder, Somatoform Disorders
Related terms Body Dysmorphic Disorders, Somatoform Disorders
Enrollment 36 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov