The Effects of e+Shots Energy Beverage on Mental Energy

Status Completed

Clinical Trial Summary

The aim of the research project is to determine the changes in motivation to perform mental and physical tasks, feelings of vigor and fatigue, mental task vigilance and fine motor function after consumption of a commercially available energy product. The purpose of this study is determine whether e+shot, a product containing natural caffeine, will impact mood and performance up to 108 minutes post consumption compared to a sweetened solution containing synthetic caffeine.

Clinical Trial Description

Enrolled participants who are low consumers of caffeine will be administered either a placebo (3mg caffeine), caffeinated placebo (~100mg of caffeine) or e+shot first and then will be crossed over to receive the other two interventions. The study consists of 3 treatment periods of 108 minutes each with a washout period of 48 hours. ;

Study Design

Related Conditions & MeSH terms

Caffeine

Clinical Trial Details

NCT number	NCT03850275
Study type	Interventional
Source	Clarkson University
Contact
Status	Completed
Phase	N/A
Start date	September 26, 2015
Completion date	December 15, 2016

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