Painrehabilitation: More is Better?
Suspended
- Conditions
- Patients with chronic musculoskeletal pain referred to a Pain Rehabilitation Program are potential participants for the study.
- Registration Number
- NL-OMON20757
- Lead Sponsor
- Center for Rehabilitation, University Medical Center Groningen (UMCG)
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Suspended
- Sex
- Not specified
- Target Recruitment
- 276
Inclusion Criteria
Patients are eligible for the study when:
1. They participate in the 12, 16 and 20 weeks Pain Rehabilitation Program (PRP) at the University Medical Centre Groningen (UMCG);
Exclusion Criteria
1. They are referred to the 8 weeks PRP;
2. They are unable to understand the Dutch language;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Self reported disability will be the main outcome and will be measured with the Pain Disability Index (scale range 0-70).
- Secondary Outcome Measures
Name Time Method Quality of life and work productivity will be secondary outcome and will be measured with respectively the Euroqol 5D and the Productivity and Disease Questionnaire (Prodisq).<br /><br>For cost-effectiveness intervention costs, other direct healthcare, direct non-healthcare and indirect costs due to absenteeism from paid work will be calculated using the handbook for economic evaluations.