RecruitingNot ApplicableNCT07565311

Two-week Intensive Outpatient Trauma Treatment.


Sponsor

Oslo University Hospital

Enrollment

42 participants

Start Date

Jan 26, 2026

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria3

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

Exclusion Criteria6

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

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Interventions

OTHERProlonged exposure and EMDR

Two-week intensive traume treatment


Locations(1)

Oslo University Hospital

Oslo, Norway

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NCT07565311


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