Patients with knee osteoarthritis scheduled for primary, unilateral total knee arthroplasty.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients diagnosed with knee osteoarthritis scheduled for primary, unilateral total knee arthroplasty at the research institute.
Exclusion criteria
Exclusion criteria: Patients who have difficulty walking independently before surgery, who deviated significantly from our clinical path due to postoperative complications, who have severe orthopedic diseases in the upper limbs or lower limbs other than the knee joint, who have neurological symptoms such as sensory impairment or motor paralysis, who have dementia or psychiatric diseases, who have serious respiratory diseases or cardiovascular diseases, and who have not consented to this research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of chronic post-surgical pain at 6 months after surgery (Visual analog scale; VAS>30mm). | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain intensity during walking (Visual analog scale; VAS), Knee joint range of motion (flexion and extension), knee joint extension muscle strength, Hospital Anxiety and Depression Scale (HADS) and Pain Catastrophizing Scale (PCS) at 1, 2 and 3 weeks and 6 months after surgery. Physical activity intensity measured by accelerometer at 1, 2 and 3 weeks after surgery. Pressure pain thresholds (PPT), Temporal summation of pain (TSP), Conditioned pain modulation (CPM), Time up and go test (TUGT) and 10-meter walk test at 2 and 3 weeks and 6 months after surgery. 6-minute walking distance and Knee Injury and Osteoarthritis Outcome Score (KOOS) at 3 weeks and 6 months after surgery. | — |
Countries
Japan
Contacts
Nagasaki University Graduate School of Biomedical Sciences Department of Physical Therapy Science, Medical and Dental Sciences