Focus of Study is to Determine Efficacy of Compex Clinical Trial
Official title:
Compex Use With Delayed Onset Muscle Soreness: A Comparison to Other Methods
The purpose of this research study is to determine if the application of ice, control group,
or a muscle stimulation program from the Compex® series can help reduce or eliminate delayed
muscle soreness from performing leg extension and flexion. Individuals will complete a
health history questionnaire to determine if they qualify for this study. We will measure
your leg girth with a measuring tape and take a pain measurement of your hamstrings by using
a spring to press down on your leg. Individuals will then warm-up on a bike without
resistance for 5 minutes followed by 10 regular leg extension and flexion exercises.
Individuals will then perform 6 sets of 10 leg extension and flexion exercises on a biodex
machine (similar to leg curl machines in the gym). Individuals will perform each set to the
maximum effort of their capables. After each set of 10 individuals will have a 2 minute
rest. We will ask you to rank your leg soreness on a scale from 1-10.
Individuals will then be assigned to a modality of either ice, control group or compex.
Individuals will perform the modality (ice, control, compex) we assign you to until you are
no longer sore.
Over the next five days individuals will return to measure their level of soreness, leg
girth and pain pressure.
This study will examine the following hypotheses:
H1: There will be no difference in pressure pain threshold after using the Compex compared
to other groups.
H2: There will be no difference in perceived soreness after using the Compex compared to
other groups.
H3: There will be no difference in muscular strength after using the Compex compared to
other groups.
H4: There will be no difference in active range of motion after using the Compex compared to
other groups.
n/a
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment