Wearable Sensors in Knee OA

Exclusion Criteria

• •Contraindication to exercise
• •Other pain in lower back or legs that is greater than knee pain
• •Currently receiving chemotherapy or radiation therapy for cancer except non-melanoma skin cancer
• •History of other disease that may involve the index joint including inflammatory joint disease such as rheumatoid arthritis, seronegative spondyloarthropathy (eg, ankylosing spondylitis, psoriatic arthritis, inflammatory bowel disease related arthropathy), crystalline disease (eg, gout or pseudogout), lupus erythematosus, knee joint infections, Paget's disease affecting the knee, or knee joint tumors.
• •Any knee surgery in the previous 6 months
• •Previous knee osteotomy, uni-compartmental replacement, or total knee replacement in either knee
• •Joint replacement in either hip or ankle
• •Planned major treatment for knee OA (e.g., surgery, injections, physical therapy) during the study period
• •Planned major surgery in the next 6 months
• •Corticosteroid or hyaluronic acid injections in either knee in the previous 3 months
• •Neurological conditions that impacts motor functioning, for e.g., stroke, Parkinson's disease, Alzheimer's disease, Multiple Sclerosis, diabetic neuropathy, etc.
• •Pregnant
• •Received physical therapy for knee OA within past 6 months
• •Known or suspected non-compliance, drug or alcohol abuse
• •Participation in another clinical trial for treatment of any joint or muscle pain
• •Participants who are investigational site staff members directly involved in the conduct of the study and their family members, site staff members otherwise supervised by the Investigators.