Effects of Energy Drink on Repeated Sprint Performance and Cognitive Function in Athletes

August 3, 2025 updated by: Chien-Wen Hou

Energy drinks are often used by athletes before competitions to enhance their performance. Recent research has pointed out that the performance effects of select ingredients have been studied individually but not in combination with caffeine. Therefore, this study is designed to investigate the effects of caffeine, anserine, and elderberry on cognitive function and repeated sprint performance of athletes during a high-intensity exercise protocol.

A double-blind, randomized crossover design will be employed. Three types of supplements will be tested: placebo, caffeine (220 mg), and an energy drink containing 220 mg caffeine, 288 mg anserine, 400 mg elderberry, and 660 mg of a vitamin-mineral mixture. Twelve college athletes will be recruited to complete repeated sprint tests on a cycle ergometer until exhaustion and to undertake a series of cognitive tasks during exercise.

Study Overview

Study Type

Interventional

Enrollment (Actual)

12

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Taipei, Taiwan, 111036
        • University of Taipei

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy adults aged 18-25
  • Currently enrolled college student
  • Active members of a collegiate wrestling team (college wrestlers)
  • Engaged in regular wrestling training
  • Willing and able to provide written informed consent
  • Agreed to maintain their usual diet and training frequency during the study period

Exclusion Criteria:

  • Individuals with known caffeine sensitivity
  • Any existing health condition that may interfere with high-intensity exercise (e.g., cardiovascular, metabolic, or neurological disorders)
  • Inability or unwillingness to follow study instructions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: Placebo Group
Participants in this group received a placebo supplement that contained no active ingredients.
Placebo powder mixed into 100 ml grape juice and 200 ml water, consumed 30 minutes before testing.
Active Comparator: Caffeine Group
Participants in this group received a caffeine supplement containing 220 mg of caffeine.
220 mg caffeine powder mixed into 100 ml grape juice and 200 ml water, consumed 30 minutes before testing.
Experimental: Energy Drink Group
Participants in this group received an energy drink containing 220 mg of caffeine, 1800 mg of anserine extract, and 400 mg of elderberry extract.
A supplement containing 220 mg caffeine, 1800 mg anserine extract, and 400 mg elderberry extract, mixed into 100 ml grape juice and 200 ml water, consumed 30 minutes before testing.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Repeated Sprint Performance
Time Frame: From second to fourth weeks, 30 minutes after the participants consumed the supplement.
Participants completed a repeated sprint test on a cycle ergometer after supplement intake and 30 minutes waiting. The test involved multiple 10-second maximal sprints with 20-second passive recoveries, continuing until fatigue (cadence < 70 rpm for over 3 seconds). During the test, the resistance was set at 0.8 Nm/kg body weight. Total power output during repeated sprint performance was the primary outcome.
From second to fourth weeks, 30 minutes after the participants consumed the supplement.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Squares performance- spatial working memory
Time Frame: From the fifth -seventh weeks, 30 minutes after the participants consumed the supplement.
The spatial memory task required participants to recall the spatial location of dots presented on a screen. A 6×6 grid was shown. First, some squares were colored for one second, and after they re-turned to normal, we need to press the squares that were previously colored. It would end if participants answered incorrectly. At higher stages, more squares were randomly colored. Reaching higher stages indicates better memory performance.
From the fifth -seventh weeks, 30 minutes after the participants consumed the supplement.
Colour drop performance- executive function
Time Frame: From the fifth -seventh weeks, 30 minutes after the participants consumed the supplement.
evaluates executive function by asking participants to name the ink color of color-words that are incongruent (e.g., the word "GREEN" printed in blue ink). Incorrect responses end the test; higher scores indicate better executive function.
From the fifth -seventh weeks, 30 minutes after the participants consumed the supplement.
Schulte grid performance- attention
Time Frame: From the fifth -seventh weeks, 30 minutes after the participants consumed the supplement.
Schulte Grid Test - measures attention by requiring participants to find numbers from 1 to 36 in ascending order on a 6×6 grid as quickly as possible; faster completion indicates better attention.
From the fifth -seventh weeks, 30 minutes after the participants consumed the supplement.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 4, 2022

Primary Completion (Actual)

May 10, 2022

Study Completion (Actual)

June 16, 2022

Study Registration Dates

First Submitted

July 1, 2025

First Submitted That Met QC Criteria

August 3, 2025

First Posted (Actual)

August 5, 2025

Study Record Updates

Last Update Posted (Actual)

August 5, 2025

Last Update Submitted That Met QC Criteria

August 3, 2025

Last Verified

June 1, 2022

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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