Cognitive behavioral therapy for long-term pain in rheumatic diseases
Evaluation of Cognitive Behavioral Therapy for Long-term Pain in Rheumatic Disease, Including Validation the Questionnaire of AE-FS
This study is testing whether cognitive behavioral therapy can help people with long-term pain from rheumatic diseases manage their pain better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Diakonhjemmet Hospital Academic / other |
| Locations | 1 site (Oslo) |
| Trial ID | NCT06413914 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of cognitive behavioral therapy (CBT) in managing long-term pain associated with rheumatic diseases. It aims to validate a Norwegian version of the Avoidance-Endurance Questionnaire (AE-FS) and explore its relationship with other questionnaires, such as the Pain Catastrophizing Scale. The intervention targets patients experiencing chronic pain and seeks to understand how CBT can facilitate changes in pain perception and coping mechanisms. The study is conducted at Diakonhjemmet Hospital in Oslo, focusing on a population with diverse rheumatic conditions.
Who should consider this trial
Good fit: Ideal candidates are individuals diagnosed with a rheumatic disorder who experience long-term pain.
Not a fit: Patients currently participating in another therapy during the study period may not benefit from this intervention.
Why it matters
Potential benefit: If successful, this approach could significantly improve pain management and quality of life for patients with rheumatic diseases.
How similar studies have performed: Previous studies have shown that cognitive behavioral therapy can be effective in managing chronic pain, suggesting a promising avenue for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * A rheumatic disorder and a long term pain condition * Written consent Exclusion Criteria: * Participation in another therapy during the study periode
Where this trial is running
Oslo
- Diakonhjemmet Sykehus — Oslo, Norway (Recruiting)
Study contacts
- Study coordinator: Kåre Osnes, PhD
- Email: kare.osnes@diakonsyk.no
- Phone: +47 92833866
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.