Study on prediction of knee pain relief by pain education and exercise
Not Applicable
- Conditions
- knee pain
- Registration Number
- JPRN-UMIN000040667
- Lead Sponsor
- Hiroshima University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
1. After knee replacement surgery 2. Those suspected of serious cognitive impairment (19 points or less on Hasegawa's simple intelligence scale) 3. Those who has received exercise therapy at a medical institution in the past but is still in severe pain (NRS score of 8 or more), has limited range of motion (-5 degree or less in extension and 125 degree or less in flexion), and is unable to walk outdoors without a cane 4. Those who are prohibited from exercising by a doctor 5. Those who were unable to obtain permission from their physicians to participate in the study 6. Those who have started exercise therapy in a medical institution within 150 days
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Knee pain Time of evaluation: Before intervention (baseline), 5 weeks, 7 weeks, and after intervention start
- Secondary Outcome Measures
Name Time Method 1. Background: sex, age, height, weight, symptoms (stiffness, crepitus, bone tenderness, swelling), complications, medical history, current medical history, medication status 2. Gait function 3. Knee joint function 4. Muscle and fat mass 5. Physical activity 6. Pain Catastrophizing 7. Fear-avoidance beliefs