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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05521347
Other study ID # 111-1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date April 30, 2022

Study information

Verified date August 2022
Source National Taiwan Sport University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date April 30, 2022
Est. primary completion date April 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 50 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Behavioral:
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.

Locations

Country Name City State
Taiwan National Taiwan University of Sport Taichung

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan Sport University

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Stroop task 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
Primary visual search test 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 aim trainer Participants used the mouse to shoot the electronic targets on the computer screen. The completed time (second) were recorded. 1 hour after intervention
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