Two-week Intensive Outpatient Trauma Treatment.

Recruiting now · Not applicable

Conditions studied: Posttraumatic Stress Disorder (PTSD)

In brief

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.

Key facts

Study ID

NCT07565311

Run by

Oslo University Hospital

People needed

42

Starts

2026-01-26

Expected to finish

2027-12-31

Last updated by the study team

2026-05-04

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• PTSD
• 18-65 years
• Able to give written informed consent.

You may not qualify if…

• Active substance abuse
• psychotic or bipolar disorder
• organic brain disorder
• IQ< 70
• Currently in a life-threating situation.
• Serious suicide risk.

Where it is running

• Oslo University Hospital — Oslo, Norway (enrolling)

Full record on ClinicalTrials.gov

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