The purpose for this protocol is to perform a double-blind, randomized, placebo-controlled, parallel-arm clinical study in healthy subjects to evaluate the efficacy of a nutraceutical product on physical and mental energy levels and overall wellness.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Enrollment
40
3 ounces daily for 8 weeks.
3 ounces daily for 8 weeks.
NIS Labs
Klamath Falls, Oregon, United States
Pain level
Pain questionnaire: Scale 0-10, with 0 being pain-free and 10 being the most pain. Change from baseline will be evaluated.
Time frame: Baseline, 2 weeks, and 8 weeks.
Range of motion
Digital inclinometry for measuring mobility of neck, back, hips, knees, and shoulders.
Time frame: Baseline and 8 weeks.
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