Clinical study on total hip arthroplasty patients with instrumented shoes
Completed
- Conditions
- Osteoarthritis in the hip/Wear and tear of hipjoint10023213
- Registration Number
- NL-OMON37965
- Lead Sponsor
- niversiteit Twente
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 25
Inclusion Criteria
•Age between 50 and 80 years.
•Primary, unilateral, osteoarthritis of the hip.
•Patients should be selected for a primary THA and undergo the operation
within the next 4 months.
Exclusion Criteria
•Have bilateral THA.
•Have any kind of leg arthroplasties.
•Have rheumatoid arthritis
•Have any neurological disorder.
•Not able to perform the tasks because of pain or impairment.
•Suffering also from other degenerative diseases.
•Develop a bilateral disease.
•Revision/re-operations of primary hip prosthesis
•Unable to understand instructions or the questionnaire
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main study parameter will be the gait velocity calculated through the IFS<br /><br>(product of the stride length and the stride frequency). </p><br>
- Secondary Outcome Measures
Name Time Method <p>Stride length and stride frequency separately as well as the symmetry in ground<br /><br>reaction force will be the secondary parameters. In addition, the IFS<br /><br>parameters correlated to the gait velocity (assessed independently from the<br /><br>IFS) and the outcome of the questionnaires (HHS, WOMAC-FC and VAS) are<br /><br>secondary parameters. </p><br>