Knee Osteoarthritis Clinical Trial
Official title:
The Effects of Knee Malalignment and Quadriceps Strengthening on the Adduction Moment in Individuals With Medial Knee Osteoarthritis
To investigate the effects of quadriceps strengthening on the adductor moment in individuals with medial knee OA and whether quadriceps strengthening has a different effect on the adductor moment in individuals with and without knee malalignment
Although quadriceps strengthening is the cornerstone of physiotherapy management, recent
evidence suggests that high quadriceps strength in patients with malaligned knees may
increase OA progression.
This study investigates the effects of quadriceps strengthening on the adduction moment in
patients with medial knee OA with and without malalignment. 107 participants with and
without varus knee malalignment were recruited and randomised into an exercise or a control
group. Participants in the exercise group were taught five quadriceps strengthening
exercises by a project physiotherapist to be performed five days a week for twelve weeks at
home. The exercises were:
1. Quadriceps exercise over fulcrum using ankle weight
2. Straight leg raise exercise using ankle weight
3. Long arc knee extension exercise in sitting using ankle weight
4. Knee extension exercise with isometric hold at 60° knee flexion using ankle weight
5. Knee extension exercise with isometric hold at 60° knee flexion using an elastic band.
Each exercise was performed at 2x10 repetitions for the first 2 weeks and 3x10 repetitions
thereafter.
Participants visited the physiotherapist 7 times at Week 1, 2, 3, 4, 5, 7 and 10. They were
given the ankle weights and elastic band to bring home and instructed about the repetitions
and weights to use by the physiotherapist, who also checked and progressed their exercises.
The average duration of the physiotherapy sessions was 30 minutes. To monitor compliance,
each participant was given an exercise instructions sheet and kept a training diary to
record the exercises they had done.
The control group received no intervention.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind, Primary Purpose: Treatment
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