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| Sponsor: | Norwegian University of Science and Technology |
|---|---|
| Collaborators: |
St. Olavs Hospital Norwegian Foundation for Health and Rehabilitation |
| Information provided by (Responsible Party): | Norwegian University of Science and Technology |
| ClinicalTrials.gov Identifier: | NCT00184301 |
Purpose
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.
| Condition | Intervention |
|---|---|
|
Eating Disorder Anorexia Nervosa Bulimia Nervosa Personality Disorder |
Behavioral: inpatient treatment Behavioral: outpatient treatment |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Treatment of Patients With Concurrent Eating Disorder and Personality Disorder: A Controlled Randomized Comparison Study, of Treatments Given to In-patients and Out-patients. |
| Estimated Enrollment: | 40 |
| Study Start Date: | September 2005 |
| Estimated Study Completion Date: | December 2012 |
| Primary Completion Date: | December 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: inpatient treatment
inpatient treatment during 1 year
|
Behavioral: inpatient treatment
inpatient treatment during 1 year
|
|
Active Comparator: outpatient treatment
intensive outpatient treatment consisting of two-weekly group sessions during 1 year
|
Behavioral: outpatient treatment
intensive outpatient treatment consisting of two-weekly group sessions during 1 year
|
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.
Eligibility| Ages Eligible for Study: | 18 Years to 45 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Norway | |
| Østmarka Psychiatric Department, St Olavs Hospital, University Hospital of Trhodheim. | |
| Trondheim, Norway | |
| Principal Investigator: | Are Holen, PhD MD | Norwegian University of Science and Technology |
More Information
| Responsible Party: | Norwegian University of Science and Technology |
| ClinicalTrials.gov Identifier: | NCT00184301 History of Changes |
| Other Study ID Numbers: | 064.03 |
| Study First Received: | September 13, 2005 |
| Last Updated: | May 11, 2012 |
| Health Authority: | Norway: Norwegian Social Science Data Services |
|
Eating disorders Anorexia nervosa Bulimia nervosa Personality disorders |
In-patient treatment out-patient treatment group therapy |
|
Anorexia Anorexia Nervosa Personality Disorders Bulimia Bulimia Nervosa |
Eating Disorders Signs and Symptoms, Digestive Signs and Symptoms Mental Disorders Hyperphagia |