Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact
Recruiting Not applicable

Feasibility of Group-Based Metacognitive Therapy for PTSD

NCT07302334 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2025-11-28
Last updated
2025-12-24

Condition(s) studied

PTSD

Investigational drug(s) / intervention(s)

Group-based metacognitive therapy

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Fulfills the diagnostic criteria for PTSD based on clinical records * Self-rated total sum score over 30 on the PCL-5 * Age ≥18 years. * Stable psychotropic medication regimen for ≥4 weeks. * Fluent in Swedish. Exclusion Criteria: * Severe psychiatric comorbidities (e.g., suicidal ideation, active psychosis, bipolar disorder) warranting immediate attention. * Current trauma-related threat (e.g., ongoing domestic violence). * Ongoing evidence-based trauma-focused psychological treatment

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)

FacilityCityRegionStatus
Affektiva, ångest och traumaprogrammet, Psykiatri Sydväst Stockholm Sweden Recruiting
Official registry record

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