Gait retraining by real-time feedback in patients with knee osteoarthritis <br>(KneeMo Feedback Study ) - KneeMo Feedback Study

Vrije Universiteit Medisch Centrum0 sites41 target enrollmentStarted: TBDLast updated: February 28, 2024

Conditions

Trial Snapshot

No summary available.

•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.

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