NCT00378248

Ullevål PersonalityProject

Ullevål PersonalityProject. A Randomized Controlled Trial of Intensive Daytreatment Followed by Outpatient Long-term Combined Treatment Compared With Eclectic Individual Therapy for Patients With Personality Disorders
Oslo University Hospital·ClinicalTrials.gov·behavioral
View on ClinicalTrials.gov
Study focus
Disease/Condition
Personality Disorders
Drug/Device/Intervention
Combined psychotherapy
Study type
Interventional
Intervention type
behavioral
Sponsor & location
Primary sponsor
Oslo University Hospital
Location
Oslo, Norway
Timeline & enrollment
Phase
N/A
Start date
May 01, 2004
End date
Dec 01, 2016
Enrollment
120 participants
Primary outcome

Psychosocial functioning,symptom distress,self esteem,interpersonal problems,,self destructive behavior,,personality pathology,,quality of life,,health care utilization after

Summary

Ullevål PersonalityProject is a ranomized controlled trial of treatment of patients with
 personality disorder. It's main purpose is to test the effect of a long-term combined
 treatment program compared with eclectic individual therapy for patients with personality
 disorders.
 
 The main study hypothesis is that long-term combined treatment is superior to eclectic
 individual therapy with respect to improvement in personality functioning, psychosocial
 functioning, symptoms, interpersonal problems, and self destructive behavior for poorly
 functioning patients with personality disorders.

ICD-10 classifications
Specific personality disordersOther specific personality disordersPersonality disorder, unspecifiedDisorders of adult personality and behaviourOther specified disorders of adult personality and behaviour
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT00378248
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT00378248 through Pure Global AI's free database. This phase not specified trial is sponsored by Oslo University Hospital and is currently status unknown. The study focuses on Personality Disorders. Target enrollment is 120 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.