Family History and Genetics |
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Clinical Trial: Effectiveness of Family-Based Versus Individual Psychotherapy in Treating Adolescents with Anorexia Nervosa
This study is currently recruiting patients.
Verified by National Institute of Mental Health (NIMH) September 2005
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Purpose
| Condition | Intervention | Phase |
|---|---|---|
| Eating Disorders | Behavior: Family therapy and individual therapy | Phase I |
MedlinePlus related topics: Eating Disorders
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study
Official Title: Treatment of Adolescents with Anorexia Nervosa
Expected Total Enrollment: 120
Study start: October 2004
In adolescents, anorexia nervosa severely affects physical, emotional, and social development. Despite the seriousness and prevalence of adolescent anorexia nervosa, few studies have focused on the effectiveness of various types of psychotherapy treatment. Family-based therapy may be an effective approach to treating adolescent anorexia nervosa. This study will compare the effectiveness of family-based therapy versus ego-oriented individual psychotherapy for the treatment of adolescent anorexia nervosa. Simultaneously, it will examine potential predictors, mediators, and moderators of weight gain, psychological concerns about weight and shape, and changes in family functioning.
Participants in this open-label study will be randomly assigned to receive one of two types of therapy: family-based therapy or ego-oriented individual psychotherapy. Both types of therapy will be given for a total of 24 hours over the course of 12 months. Physical and psychological assessments will be completed during study visits at baseline, immediately post-treatment, six months post-treatment, and one year post-treatment. Amount of weight gain will be evaluated, along with changes in weight and body shape concerns, as measured by the Eating Disorder Examination.
Eligibility
Inclusion Criteria:
- Meets DSM-IV criteria for anorexia nervosa
- Lives with at least one parent who is willing to participate
- Medically stable
- Adequate transportation to clinic
- Proficient at speaking, reading, and writing English
Exclusion Criteria:
- Currently undergoing treatment or taking medication that may affect eating or weight
Location and Contact Information
Illinois
The University of Chicago, Pritzker School of Medicine, Chicago, Illinois, 60637, United States; Recruiting
Daniel le Grange, PhD, Principal Investigator
James D. Lock, MD, PhD, Principal Investigator, Stanford University
More Information
Last Updated: September 7, 2005
Record first received: September 6, 2005
ClinicalTrials.gov Identifier: NCT00149786
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-09-13

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