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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT00272545
Date of registration: 04/01/2006
Prospective Registration: No
Primary sponsor: Drexel University
Public title: Effectiveness of a Normalization of Eating Intervention Program for Treating Women With Eating Disorders
Scientific title: Adaptation of a CBT Intervention for Eating Disorders
Date of first enrolment: January 2006
Target sample size: 280
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00272545
Study type:  Interventional
Study design:  Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment  
Phase:  N/A
Countries of recruitment
United States
Contacts
Name:     Michael R. Lowe, PhD
Address: 
Telephone:
Email:
Affiliation:  Drexel University
Key inclusion & exclusion criteria

Inclusion Criteria:

- Diagnosis of an eating disorder or eating disorder not otherwise specified (except
for binge eating disorder), as defined by the Diagnostic and Statistical Manual of
the American Psychiatric Association

- Agrees to remain in IOP treatment for at least 3 weeks

- Seeking treatment in one of the Renfrew Center's outpatient programs located in the
Philadelphia area

Exclusion Criteria:

- Diagnosis of eating disorder not otherwise specified, including binge eating disorder

- Diagnosis of a psychotic disorder

- Transferred to inpatient treatment during the IOP stay because of worsening health



Age minimum: 15 Years
Age maximum: 40 Years
Gender: Female
Health Condition(s) or Problem(s) studied
Eating Disorders
Intervention(s)
Behavioral: Normalization of Eating (NOE)
Behavioral: Treatment As Usual (TAU)
Primary Outcome(s)
Structured Clinical Interview [Time Frame: Measured at baseline]
Body weight [Time Frame: Measured at baseline, discharge, and 6 month follow-up]
Self-report [Time Frame: Measured at baseline, discharge, and 6 month follow-up]
Eating Disorders Examination [Time Frame: Measured at baseline, discharge, and 6 month follow-up]
Secondary Outcome(s)
Secondary ID(s)
R34 MH071691
R34MH071691
DATR A2-AIR
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
National Institute of Mental Health (NIMH)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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