Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07565311

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

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with Posttraumatic Stress Disorder (PTSD)
  • Aged between 18 and 65 years
  • Able to provide written informed consent
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Oslo University Hospital

Oslo, Norway

Actively Recruiting

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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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Two-week Intensive Outpatient Trauma Treatment. | DecenTrialz