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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00184301
Other study ID # 064.03
Secondary ID
Status Completed
Phase N/A
First received September 13, 2005
Last updated March 28, 2017
Start date September 2005
Est. completion date October 2013

Study information

Verified date March 2017
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date October 2013
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Anorexia nervosa, bulimia nervosa, personality disorder.

Exclusion Criteria:

- male, schizophrenia.

Study Design


Intervention

Behavioral:
inpatient treatment
inpatient treatment during 1 year
outpatient treatment
intensive outpatient treatment consisting of two-weekly group sessions during 1 year

Locations

Country Name City State
Norway Østmarka Psychiatric Department, St Olavs Hospital, University Hospital of Trondheim. Trondheim

Sponsors (3)

Lead Sponsor Collaborator
Norwegian University of Science and Technology Norwegian Foundation for Health and Rehabilitation, St. Olavs Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Score on personality, interpersonal, eating disorder and symptom scales 2 years
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