Actively Recruiting
Efficacy of Internet-delivered Trauma-focused CBT for Young People With PTSD
Led by Karolinska Institutet · Updated on 2024-03-13
240
Participants Needed
1
Research Sites
199 weeks
Total Duration
On this page
Sponsors
K
Karolinska Institutet
Lead Sponsor
C
Child and Adolescent Psychiatry, Stockholm
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to compare therapist-guided internet delivered trauma-focused cognitive behavior therapy (CBT) to an active control condition comprising therapist-guided internet delivered cognitive behavioral therapy containing relaxation techniques and psychoeducation for young people with post-traumatic stress disorder regarding efficacy and cost effectiveness. Young people with post-traumatic stress disorder will be randomly assigned to receive either 12 weeks of therapist-guided internet delivered trauma-focused cognitive behavior therapy (iTF-CBT) or therapist-guided internet delivered cognitive-behavioral therapy containing relaxation and psychoeducation.
CONDITIONS
Official Title
Efficacy of Internet-delivered Trauma-focused CBT for Young People With PTSD
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged between 13 and 17 years
- Primary diagnosis of post-traumatic stress disorder (PTSD)
- Fluent in Swedish
- Access to the internet at home or can use vouchers for internet access on a phone
- Parent or guardian willing and able to take part in treatment
You will not qualify if you...
- PTSD is not the primary concern
- Started or changed 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 clinical attention
- Receiving trauma-focused CBT or Eye Movement Desensitization and Reprocessing therapy currently
- Experiencing ongoing trauma-related threat
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Barn och ungdomspsykiatrin, BUP Internetenhet and Save the Children
Stockholm, Sweden
Actively Recruiting
Research Team
M
Maria Bragesjö
CONTACT
E
Erica Mattelin
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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