Body Dysmorphic Disorder
Conditions
Keywords
Pediatric, Body Dysmorphic Disorder, BDD, CBT, Cognitive-Behavioral Therapy
Brief summary
The purpose of this study is to develop and test the effectiveness of Cognitive-Behavioral Therapy (CBT) for children and adolescents suffering from Body Dysmorphic Disorder.
Detailed description
The main purpose of this trial is to develop and investigate the effects of a CBT protocol for children and adolescents with BDD. It is important to investigate CBT in this population given the disorder's early onset and poor trajectory if left untreated. In the first phase of this trial, we will develop the treatment manual, adapting the adult manual for use in a pediatric population. In the second phase of this trial we will test the effectiveness of the CBT treatment in 12 pediatric BDD patients. We intend to treat 12 children and adolescents with BDD. All patients will receive CBT. We will also examine treatment feasibility and acceptability (e.g., retention and reasons for treatment refusal and dropout, expectancy, and motivation), and we will explore predictors of outcome. Therapeutic progress will be broadly assessed with measures of beliefs, behaviors, mood, functioning, and quality of life before, during, and after treatment.
Interventions
BEHAVIORALCognitive-Behavioral Therapy
20 sessions of Cognitive-Behavioral Therapy
Sponsors
Massachusetts General Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
10 Years to 17 Years
Healthy volunteers
No
Inclusion criteria
* Diagnosis of DSM-IV BDD or its delusional variant, which must be present currently and for at least 6 months prior to study entry * Total score of at least 24 on the 12-item BDD-YBOCS, adolescent version, which includes a score of at least 2 on item 1 (1-3 hours/day of preoccupation with the perceived defect) * Score of at least moderate on the Clinical Global Impressions of Severity (CGI-Severity) * Score of \< 60 on the Child Global Assessment Scale (C-GAS) * Ability to communicate meaningfully with the investigators and competent to provide written assent; both parental informed consent and adolescent assent must be obtained
Exclusion criteria
* Alcohol or substance abuse or dependence within the past 3 months, bipolar disorder, psychosis, organic mental disorder, development disorder, body image concerns accounted for primarily by an eating disorder or weight concerns. If subjects have another comorbid diagnosis, the BDD has to be the primary concern. * Recent (within the past 6 months) suicide attempt, or suicidal ideation as indicated by a K-SADS score of 4 or higher that is active or warrants consideration of hospitalization * Need for inpatient or partial hospital treatment * Current psychotherapy and failure to benefit from ten or more sessions of previous CBT treatment * Participants can be receiving psychotropic medication, but they must be on a stable dose for 2 months prior to the study baseline assessment and maintain this dosage throughout the course of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Yale-Brown Obsessive Compulsive Scale Modified for BDD (BDD-YBOCS)-Pediatric Version | Baseline, Monthly, Post-Treatment, 3-Month Follow-Up, 6-Month Follow-Up |
Secondary
| Measure | Time frame |
|---|---|
| Brown Assessment of Beliefs Scale (BABS)-Pediatric Version | Baseline, Monthly, Post-Treatment, 3-Month Follow-Up, 6-Month Follow-Up |
| Clinical Global Impression Scale (CGI) | Baseline, Monthly, Post-Treatment, 3-Month Follow-Up, 6-Month Follow-Up |
| Children's Depression Inventory (CDI) | Baseline, Weekly, Post-Treatment, 3-Month Follow-Up, 6-Month Follow-Up |
Countries
United States
Outcome results
None listed