Table 3.
Outcome measures in the EXERPHARMA trial
Collection time points | |
---|---|
Primary end point | |
Knee biomechanics (mean ±95% CI): | 0, 8 weeks |
Knee index, during gait | |
Secondary end points: | |
Knee biomechanics (mean ±95% CI): | 0, 8 weeks |
Knee Index, during one-leg rise | |
Peak Knee Adduction Moment, during gait | |
Peak Knee Adduction Moment, during one-leg rise | |
Knee Adduction Moment Impulse, during gait | |
Knee Adduction Moment Impulse, during one-leg rise | |
Functional performance test (mean ±95% CI): | 0, 8 weeks |
Maximum one-leg rises from stool | |
Maximum number of knee-bendings in 30-second test | |
One-leg hop for distance test | |
Patient-reported outcomes: | |
Mean KOOS subscale scores (mean ±95% CI): | 0, 8, 52 weeks |
Pain | |
Other symptoms | |
Activities of Daily Living (ADLs) | |
Sport and Recreation Function | |
Knee-related Quality of Life (QOL) | |
Activity level: | |
UCLA activity score, change from baseline | 0, 8, 52 weeks |
Pain level: | |
Pain-level text messages, intensity (0–4) | During treatment |