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Clinical Trials/NCT00755391
NCT00755391
Completed
Not Applicable

Cognitive Behavioral Therapy for Adolescents With Bulimia

New York State Psychiatric Institute1 site in 1 country8 target enrollmentFebruary 2008
ConditionsBulimia Nervosa

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bulimia Nervosa
Sponsor
New York State Psychiatric Institute
Enrollment
8
Locations
1
Primary Endpoint
Eating Disorder Examination scores
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

This pilot study will evaluate the effectiveness of individual cognitive behavioral therapy (CBT) and supportive psychotherapy (SP) in reducing bulimic symptoms among adolescents.

Detailed Description

Patients will be randomized to have an equal chance of either receiving CBT or SP. Participants will include both individuals with DSM-IV bulimia nervosa (BN), and patients with sub-threshold BN. Adolescent patients will be treated at the New York State Psychiatric Institute, with a target recruitment of 20 patients completing the study. Participants in both conditions will be assessed prior to treatment and at the end of treatment. This trial is intended to serve as a pilot investigation to determine the feasibility and utility of a larger controlled study in this population.

Registry
clinicaltrials.gov
Start Date
February 2008
End Date
February 2010
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age between 12 and 18
  • DSM-IV diagnosis of bulimia nervosa or sub-threshold bulimia nervosa (binge eating and/or purging at least once per week)

Exclusion Criteria

  • Diagnosis of bipolar disorder
  • Current psychosis
  • Drug or alcohol abuse in the past 3 months
  • Acute Suicidal Risk
  • Major depression producing significant functional impairment
  • Significant medical illness
  • Weight outside of normal weight range (between 85% and 120% of the 50th percentile for age as measured by standard growth charts)

Outcomes

Primary Outcomes

Eating Disorder Examination scores

Time Frame: 28 days

Study Sites (1)

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