PaTIO study : PhysiotherApeutic Treat-to-target Intervention after Orthopaedic surgery; A cost-effectiveness study.
- Conditions
- hip and knee replacementtotal hip and knee arthroplasty10023213
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 624
Patients eligible for this trial are patients with clinical and radiological
knee or hip OA who are scheduled for a primary TKA or THA, and willing to
comply with the study protocol.
A potential subject who meets any of the following criteria will be excluded
from participation in this study: TKA or THA for a diagnosis other than OA,
uncontrolled cardiovascular disease or hypertension, history of neuromuscular
disorder that affects lower extremity function, terminal illness, plans to have
another joint replacement during study follow-up, not able to attend follow-up
measurements, not able to attend the PPT in primary setting, serious adverse
events during surgery or directly thereafter, serious psychiatric disorders, or
insufficient command of the Dutch language, spoken and/or written.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Difference between both groups regarding changes of KOOS-PS/HOOS-PS, a measure<br /><br>of physical functioning, between<br /><br>baseline and 3 months postoperatively.<br /><br>Differences between both groups regarding cost-effectiveness. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Differences between both groups in:<br /><br>- recovery of function during 12 months follow-up,<br /><br>- in scores of OKS/OHS (functioning), NRS (amount of pain), EQ-5D (quality of<br /><br>life), performance tests, physical activity level, and satisfaction of the<br /><br>patient. </p><br>