Actively Recruiting
Two-week Intensive Outpatient Trauma Treatment.
Led by Oslo University Hospital · Updated on 2026-05-04
42
Participants Needed
1
Research Sites
100 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The objective of the study is to obtain knowledge about the treatment of patients who are offered intensive trauma treatment at Nydalen DPS (NDPS) and Søndre Oslo DPS (SODPS). The treatment takes place on an outpatient basis over two weeks. Up to 42 patients will be recruited. The efficacy of treatment will be investigated using validated self-report forms, which measure PTSD symptoms (PCL-5 and ITQ) and quality of life/function (WHO-5, and WSAS). The measurements will be done before the treatment and one and twelve weeks after treatment.In-depth interviews will also be conducted with up to 30 patients to investigate the outcome and any need for adjustments with focus on patients with minority backgrounds, men and patients with limited benefit. The study uses a mixed methods design, where quantitative measures and information from qualitative interviews are combined to map participants' experience, benefits and feasibility.
CONDITIONS
Official Title
Two-week Intensive Outpatient Trauma Treatment.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with Posttraumatic Stress Disorder (PTSD)
- Aged between 18 and 65 years
- Able to provide written informed consent
You will not qualify if you...
- Active substance abuse
- Diagnosis of psychotic or bipolar disorder
- Organic brain disorder
- IQ less than 70
- Currently in a life-threatening situation
- Serious suicide risk
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Oslo University Hospital
Oslo, Norway
Actively Recruiting
Research Team
J
Julie H Evensen, MD PhD
CONTACT
V
Veronica Vaage-Kowalzik, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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