Two-week Intensive Outpatient Trauma Treatment.

Recruiting N/A Interventional Study
Posttraumatic Stress Disorder (PTSD)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 65
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
42 (estimated)
Sponsor
Oslo University Hospital · Other
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About This Trial
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 I…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * PTSD * 18-65 years * Able to give written informed consent. Exclusion Criteria: * Active substance abuse * psychotic or bipolar disorder * organic brain disorder * IQ\< 70 * Currently in a life-threating situation. * Serious suicide risk.
Contacts

Julie H Evensen, MD PhD

004799339292

uxevej@ous-hf.no

CONTACT

Veronica Vaage-Kowalzik, MD

UXVAAG@ous-hf.no

CONTACT