Fast track rehabilitation after reversed total shoulder arthroplasty
Recruiting
- Conditions
- shoulder complaints based on omarthrosis, rotator cuff arthropathy, avascular necrosis and (late) post traumatic
- Registration Number
- NL-OMON25527
- Lead Sponsor
- Board of directors Dijklander Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
• 50 years and older
• Selected for rTSA surgery
• Complete understandig of the study and signed informed consent
Exclusion Criteria
• Selected for rTSA with the indication of fracture treatment after an acute trauma
• Individuals who are unable to follow an intense mobilization program.
• Individuals who are unable to complete the PROMs questionnaires.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary study parameter is the difference in Oxford Shoulder Score (OSS) from preoperative to 6 weeks postoperative.
- Secondary Outcome Measures
Name Time Method Secondary study parameters are:<br>1. Difference in (ROM), VAS pain scores in rest and during activity and the quality of life (EQ-5D) from preoperative to 6 weeks postoperative.<br>2. Difference in OSS, (ROM), VAS pain scores in rest and during activity and the quality of life (EQ-5D) from preoperative to 3 months postoperative<br>3. Difference in OSS, (ROM), VAS pain scores in rest and during activity and the quality of life (EQ-5D) from preoperative to 1 year postoperative<br>4. Complications and re-admissions until 1 year postoperative.<br>5. Society costs including healthcare costs, patient and family costs and lost productivity costs.