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A Comparison Study of Treatments Given to Patients With Concurrent Eating Disorder and Personality Disorder.

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00184301
First Posted: September 16, 2005
Last Update Posted: March 29, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
St. Olavs Hospital
Norwegian Foundation for Health and Rehabilitation
Information provided by (Responsible Party):
Norwegian University of Science and Technology
September 13, 2005
September 16, 2005
March 29, 2017
September 2005
December 2011   (Final data collection date for primary outcome measure)
Score on personality, interpersonal, eating disorder and symptom scales [ Time Frame: 2 years ]
Score on personality,interpersonal, eatingdisorder and symptom scales
Complete list of historical versions of study NCT00184301 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
A Comparison Study of Treatments Given to Patients With Concurrent Eating Disorder and Personality Disorder.
Treatment of Patients With Concurrent Eating Disorder and Personality Disorder: A Controlled Randomized Comparison Study, of Treatments Given to In-patients and Out-patients.
The aim of this study is to determine whether in-patient treatment is better then intensive out-patient group treatment for patients with concurrent eating disorder and personality disorder.
The main aim of the study is to compare the effects of in-patient treatment with a group based intensive out-patient treatment. It is a randomized controlled comparison study including patients with concurrent eating disorder and personality disorder. 18 patients will receive an in-patient treatment lasting one year. 18 patients will receive intensive out-patient treatment consisting of two-weekly group sessions, lasting one year. Personality disorder, eating behavior, symptoms, and function will be followed for two years.
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Prevention
  • Eating Disorder
  • Anorexia Nervosa
  • Bulimia Nervosa
  • Personality Disorder
  • Behavioral: inpatient treatment
    inpatient treatment during 1 year
  • Behavioral: outpatient treatment
    intensive outpatient treatment consisting of two-weekly group sessions during 1 year
  • Experimental: inpatient treatment
    inpatient treatment during 1 year
    Intervention: Behavioral: inpatient treatment
  • Active Comparator: outpatient treatment
    intensive outpatient treatment consisting of two-weekly group sessions during 1 year
    Intervention: Behavioral: outpatient treatment
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
43
October 2013
December 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Anorexia nervosa, bulimia nervosa, personality disorder.

Exclusion Criteria:

  • male, schizophrenia.
Sexes Eligible for Study: Female
18 Years to 45 Years   (Adult)
No
Contact information is only displayed when the study is recruiting subjects
Norway
 
 
NCT00184301
064.03
No
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Plan to Share IPD: No
Norwegian University of Science and Technology
Norwegian University of Science and Technology
  • St. Olavs Hospital
  • Norwegian Foundation for Health and Rehabilitation
Principal Investigator: Are Holen, PhD MD Norwegian University of Science and Technology
Norwegian University of Science and Technology
March 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP