Feasibility of Group-Based Metacognitive Therapy for PTSD
Condition(s) studied
Investigational drug(s) / intervention(s)
Group-based metacognitive therapy: Group-based metacognitive therapy will be offered for 14 weeks.
Study summary
The primary objective of this study is to investigate the feasibility and acceptability of group-based Metacognitive Therapy (MCT) for post-traumatic stress disorder (PTSD) when delivered within routine psychiatric care in Sweden.
The secondary objective is to evaluate preliminary treatment effects of group-based MCT on symptoms of post-traumatic stress, complex PTSD, depression, and quality of life, and to compare treatment dropout rates to those reported in the existing literature on exposure-based treatments for PTSD.
Eligibility
Primary outcome measure(s)
- The proportion of participants that conducts the weekly measures and further assessment points — Through study completion up to the 6 months follow up
The proportion of participants that conducts the weekly measures and further assessment points - The proportion of participants that go through the entire treatment period — Completion of treatment period, up to the last session delivered 14 weeks after treatment start
The proportion of participants that go through the entire treatment period - Adverse events related to the treatment — Through study completion, up to the 6 months follow up
Adverse events related to the treatment - Acceptability — Completion of treatment period, up to the last session delivered 14 weeks after treatment start
Number of drop-outs from treatment - Treatment acceptability — Baseline
Number of individuals offered the intervention but declined part of treatment - Treatment acceptability — Up to 6 months after treatment completion
Participants experience/satisfaction with treatment and assessment procedures through qualitative interviews - Participants satisfaction with treatment, assessed by The Client Satisfaction Questionnaire (CSQ-8). — Up till treatment completion, 14 weeks after treatment start
The CSQ-8 yields a single score measuring a single dimension of overall satisfaction. An "overall score" is calculated by summing the score on each of the eight scale item. Scores range from 8 to 32, with higher values indicating higher satisfaction. - Treatment adherence — Up to treatment completion, 14 weeks after treatment start.
The proportion of completed group-sessions
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Affektiva, ångest och traumaprogrammet, Psykiatri Sydväst | Stockholm | Sweden | Recruiting |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07302334 on ClinicalTrials.gov ↗ ← All trials in Sweden