Validation of PROMIS pain interference and physical functioning in patients undergoing total hip and total knee arthroplasty
- Conditions
- Total Hip Arthroplasty (THA) or Total Knee Arthroplasty (TKA)
- Registration Number
- NL-OMON19972
- Lead Sponsor
- St. Antonius Ziekenhuis Utrecht
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 400
Inclusion Criteria
Age =18 years
-Primary arthroplasty
- Total hip arthroplasty: pre-operatively, 3, 6 or 12 months post-operatively
- Total knee arthroplasty: pre-operatively, 6 or 12 months post-operatively.
Exclusion Criteria
-Unicondylar knee arthroplasty
-Hip arthroplasty after femoral neck fracture
-Unable to independently fill out questionnaires
-Insufficient knowledge of the Dutch language
-No internet facilities
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Smallest detectable change of the PROMIS-CAT, PROMIS–Shortforms and the currently used outcome measurement instruments in patients undergoing THA or TKA
- Secondary Outcome Measures
Name Time Method Psychometric properties of the PROMIS-CAT, PROMIS-Shortforms and the currently used outcome measurement instruments in patients undergoing THA or TKA<br>o Reliability<br>o Internal consistency<br>o Measurement error<br>o Construct validity<br>o Responsiveness<br>- Burden for patients (the number of items needed)<br>- Interpretability of the scores