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Effectiveness of Family-Based Versus Individual Psychotherapy in Treating Adolescents with Anorexia Nervosa - Article


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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

Sponsors and Collaborators: National Institute of Mental Health (NIMH)
University of Chicago, Pritzker School of Medicine
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00149786

Purpose

This study will compare the effectiveness of family-based therapy versus individual psychotherapy for the treatment of adolescent anorexia nervosa.
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

Further Study Details: 
Primary Outcomes: Weight increase to 90% or higher from baseline to end of treatment; Scores on the Eating Disorders Examination from baseline to end of treatment
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

Ages Eligible for Study:  12 Years   -   18 Years,  Genders Eligible for Study:  Both
Criteria

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

Please refer to this study by ClinicalTrials.gov identifier  NCT00149786

Judy G. Beenhakker, MS      650-723-7885    judybeen@stanford.edu

Illinois
      The University of Chicago, Pritzker School of Medicine, Chicago,  Illinois,  60637,  United States; Recruiting
Kristen Hewell  773-834-5677    khewell@yoda.bsd.uchicago.edu 
Daniel le Grange, PhD,  Principal Investigator

Study chairs or principal investigators

James D. Lock, MD, PhD,  Principal Investigator,  Stanford University   

More Information

Study ID Numbers:  MH70621-01
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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Page Updated: September 6, 2005
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