- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06621797
Effects of Caffeine, L-Theanine, and Diaphragmatic Breathing on Esports Players' Performance (CLD Esports St)
Can L-Theanine Supplementation or Diaphragmatic Breathing Exercises in Addition to Caffeine Supplementation Be Used as Ergogenic Aids to Influence Game Performance in Esports Players?
Study Overview
Status
Conditions
Detailed Description
This study explores the effects of caffeine, L-theanine supplementation, and diaphragmatic breathing exercises on esports players' game performance, focusing on reaction time and accuracy. Caffeine is widely recognized for its stimulating effects, improving attention and reducing fatigue, while L-theanine, found in tea, is known to reduce stress and balance the effects of caffeine. Diaphragmatic breathing exercises are designed to lower stress levels, improve focus, and enhance cognitive function.
The study utilizes a randomized, single-blind crossover design, where participants-esports players aged 18-30-will undergo three different interventions: caffeine only, caffeine combined with L-theanine, and caffeine combined with diaphragmatic breathing exercises. Performance outcomes, including reaction time and accuracy, will be assessed using game-based software and tests. Participants will have their performance measured before and after each intervention, allowing for comparison between the different strategies.
This study aims to determine whether these supplements and exercises, alone or in combination, can serve as effective ergogenic aids, helping esports players optimize their performance by improving cognitive and motor skills, while also reducing stress. These findings could have broader applications for enhancing mental performance in competitive environments.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Balıkesir, Turkey
- Bandirma Onyedi Eylül University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male esports players aged 18-30.
- Actively involved in esports for at least 6 hours per week for a minimum of 6 months.
- Low caffeine consumption (less than 80 mg per day).
- Low L-theanine consumption (less than 100 mg per day).
- Non-smokers or those who do not use tobacco products.
- No recent history of upper extremity surgery.
- No known allergies to caffeine or L-theanine.
- No neurological, visual, or auditory disorders.
- No use of drugs or performance-enhancing supplements within the past month.
- No alcohol consumption within the past week.
Exclusion Criteria:
- Use of stimulant medications.
- History of upper extremity surgery.
- Diagnosed neurological, visual, or auditory disorders.
- Allergy to caffeine or L-theanine.
- Use of drugs or performance-enhancing supplements within the past month.
- Regular tobacco use.
- Consumption of alcohol in the past week.
- Inconsistent sleep patterns or difficulty following standardized sleep and hydration guidelines.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Caffeine Only Arm
Participants receive a caffeine supplement only.
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Participants in this group will receive a caffeine supplement (3 mg/kg body weight) taken orally 45 minutes before performance testing.
No additional interventions will be administered.
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Experimental: Caffeine + L-Theanine Arm
Participants receive a combination of caffeine and L-theanine supplements.
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Participants in this group will receive a caffeine supplement (3 mg/kg body weight) along with L-theanine in a 1:2 ratio taken orally 45 minutes before performance testing.
|
|
Experimental: Caffeine + Diaphragmatic Breathing Exercises Arm
Participants receive a caffeine supplement and perform diaphragmatic breathing exercises.
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Participants in this group will receive a caffeine supplement (3 mg/kg body weight) 45 minutes before performance testing, followed by a 10-minute session of diaphragmatic breathing exercises.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reaction Time
Time Frame: Reaction time will be assessed immediately before each intervention and at two time points after each intervention (at 45 minutes and 2 hours post-intervention) on each of the three study days.
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The time it takes for participants to respond to visual and auditory stimuli during gaming, measured in milliseconds using Aim Lab and other standardized reaction time tests.
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Reaction time will be assessed immediately before each intervention and at two time points after each intervention (at 45 minutes and 2 hours post-intervention) on each of the three study days.
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Pathologic Processes
- Respiratory Tract Diseases
- Respiration Disorders
- Respiratory Aspiration
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Enzyme Inhibitors
- Purinergic Antagonists
- Purinergic Agents
- Phosphodiesterase Inhibitors
- Purinergic P1 Receptor Antagonists
- Central Nervous System Stimulants
- Caffeine
Other Study ID Numbers
- Hacettepe123
- 123456789 (Bandirma Onyedi Eylul University)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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