Gait retraining by real-time feedback in patients with knee osteoarthritis <br>(KneeMo Feedback Study )
- Conditions
- osteoarthritis10023213
- Registration Number
- NL-OMON43704
- Lead Sponsor
- Vrije Universiteit Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 41
Inclusion criteria for the present study (A and B) are knee osteoarthritis on the medial compartment based on the ACR criteria, age between 50 and 75 years old, Body Mass Index (BMI) between 20 and 30 kg/m2, maximum score of 7 on the numeric rate scale (NRS) for pain intensity during the past two weeks.
Additional inclusion criteria for study B is satisfaction with applied gait modification pattern in study A, willingness to further learn this pattern and clear improvement in knee adduction moment (approximately 10% reduction). This will be at the discretion of the physiotherapist involved who will have the final decision on inclusion.
Total knee replacement, rheumatoid arthritis or any other form of inflammatory arthritis (i.e., crystal arthropathy or septic arthritis). Similarly patients with hip osteoarthritis will be excluded, as will people with poor vision that would prevent them from being able to see the visual feedback. Patients who are already included in any other experimental research study (including but not limited to the Vitamin D study and the COOA study) will also be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method