high tibial osteotomy patient
Conditions
Interventions
Control group: rehabilitation alone (60 min/day, 6 times/week)
Intervention group 1: combined rehabilitation and group-style pain management education (5 sessions of 1 hour/session for a total of 5 we
Sponsors
Department of Rehabilitation, Fukuoka Rehabilitation Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) read and speak Japanese and provided informed consent (2) had a diagnosis of osteoarthritis as determined by their orthopedic surgeons, and(3) were scheduled for primary (not revision) unilateral open-wedge HTO
Exclusion criteria
Exclusion criteria: (1) scheduled for revision arthroplasty surgery (2) unable to or declined to provide consent for study participation (3) had a self-reported diagnosis of inflammatory arthritis (i.e., rheumatoid arthritis, systemic lupus erythematosus, or ankylosing spondylitis) (4) had neurological or psychological disease (5) scheduled to undergo HTO because of a fracture, malignancy, or infection (6) scheduled for bilateral HTO (7) scheduled for unilateral arthroplasty (8) reported plans to undergo hip or knee arthroplasty within 6 months after the current HTO
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain of rest and walking using the numerical rating scale at pre-operation and post-operation 5weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain catastrophizing using the pain catastrophizing scale, pain self efficacy using pain self efficacy questionnaire, pain pain management strategies using coping strategy questionnaire, 10m walking test, and isometric muscle strength at pre-operation and post-operation 5weeks | — |
Countries
Japan
Contacts
Public ContactNaoki Deguchi
Fukuoka rehabilitation hospital Department of Rehabilitation
Outcome results
None listed