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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.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00184301
Enrollment
43
Registered
2005-09-16
Start date
2005-09-30
Completion date
2013-10-31
Last updated
2017-03-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anorexia Nervosa, Bulimia Nervosa, Eating Disorder, Personality Disorder

Keywords

Eating disorders, Anorexia nervosa, Bulimia nervosa, Personality disorders, In-patient treatment, out-patient treatment, group therapy

Brief 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.

Detailed 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.

Interventions

BEHAVIORALinpatient treatment

inpatient treatment during 1 year

BEHAVIORALoutpatient treatment

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

Sponsors

St. Olavs Hospital
CollaboratorOTHER
Norwegian Foundation for Health and Rehabilitation
CollaboratorOTHER
Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Anorexia nervosa, bulimia nervosa, personality disorder.

Exclusion criteria

* male, schizophrenia.

Design outcomes

Primary

MeasureTime frame
Score on personality, interpersonal, eating disorder and symptom scales2 years

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026