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

This study is currently recruiting participants.

Verified April 2009 by Norwegian University of Science and Technology

First Received on September 13, 2005. Last Updated on April 27, 2009 History of Changes

Sponsor:	Norwegian University of Science and Technology
Collaborators:	St. Olavs Hospital Norwegian Foundation for Health and Rehabilitation
Information provided by:	Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:	NCT00184301

Purpose

The purpose for this study is to determine whether inpatient treatment is better then intensive outpatient group treatment for patients with concurrent eating disorder and personality disorder.

Condition	Intervention	Phase
Eating Disorder Anorexia Nervosa Bulimia Nervosa, Personality Disorder	Behavioral: Treatment programs	Phase I

Study Type:	Interventional
Study Design:	Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind Primary Purpose: Prevention
Official Title:	Treatment of Patients With Concurrent Eatingdisorder and Personality Disorder: A Controlled Randomized Comparison Study, of Treatments Given to Inpatients and Outpatients.

Resource links provided by NLM:

MedlinePlus related topics: Eating Disorders Personality Disorders

U.S. FDA Resources

Further study details as provided by Norwegian University of Science and Technology:

Primary Outcome Measures:

Score on personality,interpersonal, eatingdisorder and symptom scales

Estimated Enrollment:	40
Study Start Date:	September 2005
Estimated Study Completion Date:	December 2012

Detailed Description:

The main aim of the study is to compare the effects of inpatient treatment with a group based intensive outpatient treatment. It is a randomized controlled comparison study including patients with concurrent eating disorder and personality disorder. 18 patients will receive a inpatient treatment lasting one year. 18 patients will receive intensive outpatient treatment consisting of to weekly grouptratment sessions, lasting one year. Personalitydisorder, eatingbehavior, 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

Criteria

Inclusion Criteria:

Anorexia nervosa, bulimia nervosa, personalitydisorder.

Exclusion Criteria:

male, schizophrenia.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00184301

Contacts

Contact: Are Holen, PhD MD

+4773551500

Are.holen@ntnu.no

Locations

Norway
Østmarka Psychiatric Department, St Olavs Hospital, University Hospital of Trhodheim.	Recruiting
Trondheim, Norway
Contact: Are Holen, PhD MD +4773551500 are.holen@ntnu.no
Contact: Jens Dahl +4773864500 jens.dahl@ntnu.no
Principal Investigator: Are Holen, PhD MD

Sponsors and Collaborators

Norwegian University of Science and Technology

St. Olavs Hospital

Norwegian Foundation for Health and Rehabilitation

Investigators

Principal Investigator:

Are Holen, PhD MD

Norwegian University of Science and Technology

More Information

No publications provided

Responsible Party:	Professor Are Holen, 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:	April 27, 2009
Health Authority:	Norway: Norwegian Social Science Data Services

Keywords provided by Norwegian University of Science and Technology:

Eatingdisorders,
Anorexia nervosa,
Bulimia nervosa,

Personality disorders,
Inpatient treatment,
outpatient treatmet,

Additional relevant MeSH terms:

Anorexia
Anorexia Nervosa
Personality Disorders
Bulimia
Bulimia Nervosa

Eating Disorders
Signs and Symptoms, Digestive
Signs and Symptoms
Mental Disorders
Hyperphagia

ClinicalTrials.gov processed this record on February 09, 2012