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Clinical Trials in Norway / NCT07579897
Recruiting Not applicable

Group vs. Individual Metacognitive Therapy for Generalized Anxiety Disorder

NCT07579897 · tracked via the Priya Life Science Norway tracker
Phase
Not applicable
Started
2026-03-27
Last updated
2026-05-12

Condition(s) studied

Generalized Anxiety Disorder

Investigational drug(s) / intervention(s)

Individual Metacognitive TherapyGroup Metacognitive Therapy

Individual Metacognitive Therapy: Individual metacognitive therapy (MCT) is delivered by a trained clinician following the established protocol for generalized anxiety disorder. The treatment focuses on modifying maladaptive metacognitive beliefs, reducing the cognitive-attentional syndrome (CAS), and promoting flexible attentional control. Participants receive 10 weekly individual sessions, each lasting approximately 45 minutes. The intervention targets excessive worry, unhelpful coping strategies, and beliefs about the uncontrollability and danger of worry.

Group Metacognitive Therapy: Group Metacognitive Therapy (g-MCT) is delivered by two trained clinicians following the established group MCT protocol for generalized anxiety disorder. Treatment is provided in small groups of 4-6 participants and focuses on modifying maladaptive metacognitive beliefs, reducing the cognitive-attentional syndrome (CAS), and improving attentional flexibility. Participants attend 10 weekly sessions, each lasting approximately 90 minutes.

Study summary

Generalized anxiety disorder (GAD) is a serious and long-lasting condition that can greatly reduce quality of life, work functioning, and use of health services. Metacognitive therapy (MCT) is an effective treatment for GAD, but it is not yet known whether individual MCT or group-based MCT provides the best results for patients.

This randomized controlled trial will compare two formats of MCT: individual treatment and group-based treatment (g-MCT). A total of 64 adults with GAD (32 in each treatment arm) will participate after providing informed consent. Participants will complete questionnaires, undergo clinical assessments, and allow the study to collect relevant health information from official registries.

The main aim of the study is to determine whether group-based MCT is non-inferior to individual MCT. A non-inferiority design tests whether the group format is not meaningfully less effective than the individual format. If group MCT is shown to have similar effects on anxiety symptoms and functioning, it could offer an efficient and resource-saving alternative in routine clinical care.

This will be the first study to systematically compare these two treatment formats in a real-world clinical setting. If group MCT proves to be as effective as individual therapy, it may help increase access to evidence-based treatment for people with GAD, reduce strain on mental health services, and support the development of more accessible and cost-effective care.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Adults with a primary diagnosis of generalized anxiety disorder (GAD). GAD-7 score ≥ 10 at screening/baseline. Participants must endorse that they experience problems with excessive worry Exclusion Criteria: 1. Bipolar disorder; 2. Psychosis; 3. Ongoing substance abuse/dependence; 4. Intellectual disability based on previous medical history; 5. Eating disorder in need of medical attention; 6. Unwillingness to refrain from anxiolytic drugs during the treatment; 7. Current suicidal ideation with plan and intent; 8. Taking an unstable dose of antidepressant, with recent dose-change within the last 4 weeks; 9. Known cluster A or B personality disorder; 10. Serious medical comorbidity (e.g.: cancer, severe renal failure) 11. Language difficulties in need of an interpreter.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Sørlandet Hospital HF Kristiansand Agder Recruiting
Sørlandet Hospital HF Kristiansand Norway Recruiting

More Sorlandet Hospital HF trials in Norway

Other trials for the same condition

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 NCT07579897 on ClinicalTrials.gov ↗ ← All trials in Norway