- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05881018
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
Status
Not yet recruiting
Conditions
Intervention / Treatment
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.
Sponsor
Collaborators
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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