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RECRUITING
NCT07565311
NA

Two-week Intensive Outpatient Trauma Treatment.

Sponsor: Oslo University Hospital

View on ClinicalTrials.gov

Summary

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 Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

42

Start Date

2026-01-26

Completion Date

2027-12-31

Last Updated

2026-05-04

Healthy Volunteers

No

Interventions

OTHER

Prolonged exposure and EMDR

Two-week intensive traume treatment

Locations (1)

Oslo University Hospital

Oslo, Norway