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Study on prediction of knee pain relief by pain education and exercise

The effects and indications of a phased intervention strategy for knee pain - Study for prediction of knee pain relief

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040667
Enrollment
80
Registered
2020-06-05
Start date
2020-06-05
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

knee pain

Interventions

Pain education (once a week, 4 weeks), gait modification (once a week, 2 weeks), and walking exercise (twice a week, 6 weeks)

Sponsors

Hiroshima University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Those with knee pain (NRS >= 2) 2. Those who has been examined by a physician, has no rheumatoid arthritis, gout, osteonecrosis of the granular femur, patellar dislocation, or any other disease that requires emergency surgery and is not prohibited from exercising. 3. Those whose written consent to participate in the study is obtained from the individual. 4. Over 50 years old 5. No limitation for gender

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Knee pain Time of evaluation: Before intervention (baseline), 5 weeks, 7 weeks, and after intervention start

Secondary

MeasureTime frame
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

Countries

Japan

Contacts

Public ContactRyo Tanaka

Hiroshima University Graduate School of Humanities and Social Sciences

ryotana@hiroshima-u.ac.jp082-454-6585

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026