Investigating the Effects of Diet and Physical Activity on Esport Performance

May 26, 2023 updated by: Beneo-Institute
A randomized, counterbalanced intervention study in esport players.

Study Overview

Detailed Description

The study will test whether i) the consumption of two different carbohydrate drinks and ii) the performance of regular high-intensity interval training will impact esport performance and metabolic profile.

Study Type

Interventional

Enrollment (Estimated)

48

Phase

  • Not Applicable

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Informed consent obtained
  • Male or female aged 18-45 years
  • Healthy
  • Participants have to be part of an esport association and/or regularly participate in tournaments

Exclusion Criteria:

  • diabetes mellitus type 1 or 2 (T1DM or T2DM)
  • medication which impacts glucose metabolism or visual perception
  • health issues like cardiovascular diseases, severe orthopaedic conditions or neurological impairments
  • food allergies or intolerances, e.g. fructose malabsorption

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Low glycaemic index
Diet will be supplemented with a drink containing a low glycaemic index carbohydrate
Experimental: Low glycaemic index with physical activity units
Diet will be supplemented with a drink containing a low glycaemic index carbohydrate
Participants will include physical activity units
Experimental: High glycaemic index
Diet will be supplemented with a drink containing a high glycaemic index carbohydrate
Experimental: High glycaemic index with physical activity units
Participants will include physical activity units
Diet will be supplemented with a drink containing a high glycaemic index carbohydrate

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in esport performance (test battery)
Time Frame: 4 weeks
Reaction time will be measured using an esport test battery
4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Glucose response (continuous glucose monitor): 3h iAUC
Time Frame: 4 weeks
The 3h incremental area under the curve (iAUC) will be used to assess glycemic response to the drink. Unit: mg/dL
4 weeks
Glycaemic variability (continuous glucose monitor): 24h MAGE
Time Frame: 4 weeks
The mean amplitude of glycemic excursion during 24h will be assessed as an indicator for glycemic variability. Unit: mg/dL
4 weeks

Collaborators and Investigators

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

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 (Estimated)

July 1, 2023

Primary Completion (Estimated)

December 1, 2023

Study Completion (Estimated)

December 1, 2023

Study Registration Dates

First Submitted

April 12, 2023

First Submitted That Met QC Criteria

May 26, 2023

First Posted (Actual)

May 30, 2023

Study Record Updates

Last Update Posted (Actual)

May 30, 2023

Last Update Submitted That Met QC Criteria

May 26, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • ES01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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