Caffeine+TeaCrine+Dynamine
Drugcombination of caffeine, TeaCrine, and Dynamine
Other names: Combination
NCT Number: NCT03937687
The purpose of this randomized, placebo-controlled, three-condition, double-blind, between-subjects clinical trial is to determine and compare the effects of the combination of TeaCrine®, Dynamine, and caffeine to a placebo and caffeine condition on reaction time and target acquisition and accuracy. A secondary purpose is to observe the changes in hemodynamic variables in response to this combination.
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Notify Me18 year–63 year
Male
Interventional
Early Phase 1
Rutgers University Center for Health and Human Performance, New Brunswick, New Jersey, United States
BASELINE ASSESSMENT:
CONDITIONS:
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
combination of caffeine, TeaCrine, and Dynamine
Other names: Combination
Placebo
Caffeine
Time frame: 4 minutes, following the first 30-minute mental fatigue protocol
Spatial reaction
Time frame: 4 minutes, following the second 30-minute mental fatigue protocol
Spatial reaction
Time frame: 2 minutes, following the first 30-minute mental fatigue protocol
Simulated marksmanship using optical targetry
Time frame: 2 minutes, following the second 30-minute mental fatigue protocol
Simulated marksmanship using optical targetry
Time frame: 3 hours total
Changes in blood pressure throughout the course of the protocol
Time frame: 3 hours total
Changes in heart rate throughout the course the protocol
University of South Carolina
Other
The Effects of a Combination of TeaCrine®, Dynamine, and Caffeine on Marksmanship Accuracy and Reaction Time in ROTC Members, Military, and Law Enforcement Following a Mentally Fatiguing Protocol
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.