The aim of the clinical trial is to evaluate the efficacy of two novel hydration products on rehydration following exercise.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
16
The University of Memphis
Memphis, Tennessee, United States
RECRUITINGRelative rehydration
To determine the effect of the test products (TPs) on relative rehydration after exercise, as compared to placebo via percent plasma volume change and plasma osmolality
Time frame: Through study completion, an average of 8 weeks
Hydration status via sweat loss
To determine the effect of the TPs on hydration status, as compared to placebo via sweat loss
Time frame: Through study completion, an average of 8 weeks
Participants reported outcomes
To determine the effect of the TPs on participant reported outcomes, as compared to placebo via bloating, exertion, exhaustion, thermal sensation, feeling of refreshment, stomach upset, and thirst
Time frame: Through study completion, an average of 8 weeks
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