Evaluation of the Structured Patient Information Program for Rheumatoid Arthritis (StruPI-RA)
Not Applicable
Recruiting
- Conditions
- M13Other arthritis
- Registration Number
- DRKS00015123
- Lead Sponsor
- Deutsche Gesellschaft für Rheumatologie
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 200
Inclusion Criteria
A maximum of half a year since the diagnosis of rheumatoid arthritis according to the ACR / EULAR criteria (as of 2010) or DMARD (disease modifiying antirheumatic drugs) or change of therapy. The participants should have participated in all three modules of the StruPI-RA, follow the training content and be able to complete the questionnaire independently.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Difference of patients with RA with structured outpatient training to patients of the same indication without appropriate intervention in terms of training-related criteria such as knowledge acquisition (modified PKQ), self-management (heiQ-Core), compliance (therapy cooperation) and empowerment.
- Secondary Outcome Measures
Name Time Method Improvement by StruPI-RA intervention for other outcome measures such as functional fitness (FFbH), quality of life (SF-36), work resolution (WAI), predictive earning capacity (SPE), disease activity (SJC28, TJC28; VAS physician) and drug consumption.