- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05521347
Caffeine Supplementation Improves the Cognitive Abilities and Shooting Performance of Trained E-sports Players
August 26, 2022 updated by: Chih-Hui Chiu, National Taiwan Sport University
Graduate Program in Department of Exercise Health Science, National Taiwan University of Sport
Purpose: investigators explored the effect of 3 mg/kg of caffeine supplementation on the cognitive ability and shooting performance of trained e-sports players.
Methods: investigators recruited nine e-sports players who had received professional training in e-sports and had won at least eighth place in national-level e-sports shooting competitions.
After performing three to five familiarization tests, investigators employed a randomized crossover design to divide participants into a caffeine trial (CAF) and a placebo trial (PL).
The CAF group took capsules with 3 mg/kg of caffeine, whereas the PL group took a placebo capsule.
After a 1-h rest, the Stroop task, visual search ability test, and the shooting ability test were conducted.
Study Overview
Study Type
Interventional
Enrollment (Actual)
9
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
-
-
-
Taichung, Taiwan, 404
- National Taiwan University of Sport
-
-
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
20 years to 50 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- had experience with national competitions and regularly underwent training in first-person shooters
Exclusion Criteria:
- no experience with national competitions and regularly underwent training in first-person shooters
- have any diseases affecting the heart, bones, and joints or diseases that preclude exercise
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: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: caffeine
capsules with 3 mg/kg of caffeine
|
we employed a randomized crossover design to divide participants into a caffeine trial (CAF) and a placebo trial (PL).
The CAF group took capsules with 3 mg/kg of caffeine, whereas the PL group took a placebo capsule.
After a 1-h rest, the Stroop task, visual search ability test, and the shooting ability test were conducted.
|
Placebo Comparator: placebo
The placebo capsule contained flour
|
we employed a randomized crossover design to divide participants into a caffeine trial (CAF) and a placebo trial (PL).
The CAF group took capsules with 3 mg/kg of caffeine, whereas the PL group took a placebo capsule.
After a 1-h rest, the Stroop task, visual search ability test, and the shooting ability test were conducted.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Stroop task
Time Frame: 1 hour after intervention
|
The color-word Stroop task and visual search test were conducted using Psych/Lab for Windows.
The reaction time (millisecond) were recorded.
|
1 hour after intervention
|
visual search test
Time Frame: 1 hour after intervention
|
A total of 80 search displays were presented in 5 minutes.
In each display, 5, 10, 15, or 20 -Tests were presented.
The reaction time (millisecond) were recorded.
|
1 hour after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
aim trainer
Time Frame: 1 hour after intervention
|
Participants used the mouse to shoot the electronic targets on the computer screen.
The completed time (second) were recorded.
|
1 hour after intervention
|
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 1, 2022
Primary Completion (Actual)
April 1, 2022
Study Completion (Actual)
April 30, 2022
Study Registration Dates
First Submitted
August 24, 2022
First Submitted That Met QC Criteria
August 26, 2022
First Posted (Actual)
August 30, 2022
Study Record Updates
Last Update Posted (Actual)
August 30, 2022
Last Update Submitted That Met QC Criteria
August 26, 2022
Last Verified
August 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 111-1
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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