Group therapy for patients with lasting trauma reactions
Adding a Group Based Stabilization and Skill Training Intervention for Patients With Long Lasting Posttraumatic Reactions Receiving Outpatient Treatment in Specialized Mental Health Care - A Randomized Controlled Trial
This study tests if adding group therapy to regular treatment can help people with long-lasting trauma feel better and improve their overall well-being.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 160 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | St. Olavs Hospital Academic / other |
| Locations | 1 site (Trondheim) |
| Trial ID | NCT03887559 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of adding a group-based stabilization and skill-training intervention to the standard individual outpatient treatment for patients experiencing long-lasting post-traumatic reactions. Participants will be divided into two groups, with one receiving the combined treatment and the other receiving standard care. The study aims to assess changes in mental health, functional impairment, well-being, and inflammation markers before and after the intervention. By targeting patients with complex psychological symptoms, the research seeks to develop more effective treatment options for those in community mental health care.
Who should consider this trial
Good fit: Ideal candidates are individuals receiving outpatient treatment for post-traumatic stress reactions who have experienced traumatic events and have symptoms lasting at least six months.
Not a fit: Patients with active psychotic symptoms, substance abuse issues, or high suicidal risk may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the mental health and quality of life for patients suffering from long-lasting post-traumatic reactions.
How similar studies have performed: Other studies have shown promise in using group-based interventions for trauma, suggesting potential success for this novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Receiving treatment in ordinary out-patient clinics * Having been exposed to or witnessing to traumatic event(s) defined as "one or several extremely threatening or horrific events or series of events or situations being of such a character which is likely to overwhelming distress in almost anyone in a similar situation", measured by Stressful Life Events Screening Questionnaire * Presenting with posttraumatic reactions such as hyperarousal, avoidance, intrusions, emotional dysregulation or interpersonal difficulties. * Symptom duration for a minimum of six months. * Understand and speak Norwegian to an extent that is required to participate in a stabilization- and skill-training group. Exclusion Criteria: * Active psychotic symptoms. * Substance or drug addiction or abuse. * High suicidal risk considered by the individual therapist. * Having participated in the course previously.
Where this trial is running
Trondheim
- Department of Tiller DPS, St. Olavs Hospital University Hospital in Trondheim — Trondheim, Norway (Recruiting)
Study contacts
- Study coordinator: Katrine Høyer Holgersen, PhD
- Email: katrine.hoyer.holgersen@stolav.no
- Phone: +47 72 82 39 00
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.