Actively Recruiting
Efficacy of Internet-delivered Cognitive-behavior Therapy for PTSD
Led by Karolinska Institutet · Updated on 2023-12-07
286
Participants Needed
1
Research Sites
154 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 therapist-guided internet delivered prolonged exposure to an active control condition( therapist-guided internet delivered cognitive behavioral therapy containing relaxation techniques) for post-traumatic stress disorder. The objective with this study is to investigate efficacy, mechanisms of change and cost effectiveness of therapist-guided internet delivered prolonged exposure. Adult patients with post-traumatic stress disorder will be randomly assigned to receive either 10 weeks of therapist-guided internet delivered prolonged exposure or therapist-guided internet delivered cognitive-behavioral therapy containing relaxation.
CONDITIONS
Official Title
Efficacy of Internet-delivered Cognitive-behavior Therapy for PTSD
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Current primary diagnosis of PTSD according to DSM-5 criteria
- 18 years of age or older
- Able to read and communicate fluently in Swedish
- Stable dose of any psychotropic medication for at least 4 weeks before entering the study
- Daily access to a computer or device with internet connection
You will not qualify if you...
- PTSD is not the primary concern
- Started or adjusted any psychotropic medication within 4 weeks before treatment
- Serious mental health symptoms such as mania, psychosis, alcohol or substance use disorders, or current suicide risk needing immediate care
- Currently undergoing trauma-focused CBT or Eye Movement Desensitization and Reprocessing therapy
- Experiencing ongoing trauma-related threats such as living with a violent spouse
AI-Screening
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Trial Site Locations
Total: 1 location
1
Traumaprogrammet, Psykiatri Sydväst
Stockholm, Sweden
Actively Recruiting
Research Team
M
Maria Bragesjö, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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