Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05934175

Intensive Treatment Versus Standard Weekly Prolonged Exposure for Adults With Post-Traumatic Stress Disorder

Led by Karolinska Institutet · Updated on 2026-04-07

140

Participants Needed

1

Research Sites

197 weeks

Total Duration

On this page

Sponsors

K

Karolinska Institutet

Lead Sponsor

R

Region Stockholm

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare a novel, massed treatment format of prolonged exposure to gold standard trauma focused cognitive behavioral therapy (weekly delivered prolonged exposure) for post-traumatic stress disorder. The objective with this study is to investigate efficacy, mechanisms of change and cost effectiveness of intensive prolonged exposure (I-PE) in regular Swedish psychiatric care. Adult patients with post-traumatic stress disorder will be randomly assigned to receive either gold standard prolonged exposure weekly for 15 weeks or 5 days of intensive treatment with the addition of three booster sessions dispersed 1, 2 and 4 weeks after completion of the massed treatment period. Qualitative interviews will be conducted with therapists to explore their experiences of delivering intensive treatment for PTSD, with particular focus on perceived benefits and challenges, clinical processes, patient engagement, and the impact of the intensive format on therapeutic work.

CONDITIONS

Official Title

Intensive Treatment Versus Standard Weekly Prolonged Exposure for Adults With Post-Traumatic Stress Disorder

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years of age or above
  • Primary PTSD diagnosis
  • Fluent in Swedish
  • Signed informed consent
  • Able to attend either intensive prolonged exposure or 15 weekly prolonged exposure sessions
Not Eligible

You will not qualify if you...

  • Started or changed psychotropic medication within 4 weeks before treatment
  • Serious mental health symptoms such as mania, psychosis, substance use disorders, or current suicide risk needing immediate care
  • Currently receiving evidence-based trauma-focused psychological treatment
  • Ongoing trauma-related threat, such as living with a violent spouse

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

Traumaprogrammet, Psykiatri Sydväst

Stockholm, Sweden

Actively Recruiting

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Research Team

M

Maria Bragesjö, PhD

CONTACT

H

Hannes Hedvall, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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