Effects of Caffeine on Agility in Amateur Soccer Players
Effects of Caffeine on Physical and Perceptual-cognitive Components of Agility in Amateur Soccer Players
1 other identifier
interventional
16
1 country
1
Brief Summary
This randomized, double-blind, placebo-controlled crossover clinical trial aims to investigate the acute effects of caffeine supplementation on motor and perceptual-cognitive components of agility performance in male amateur soccer players. The main questions are: i) Does acute caffeine supplementation improve motor performance, including countermovement jump height, drop-jump reactive strength, and planned agility? ii) Does acute caffeine supplementation improve perceptual-cognitive performance during reactive agility tasks involving light and human stimuli? Participants will complete two experimental conditions in randomized order, receiving either 300 mg of caffeine (\~3.7 miligrams/kilograms of body mass) or placebo pills. Following ingestion, participants will perform countermovement and drop jumps and three Y-shaped agility tests assessing planned agility, reactive agility to a light stimulus, and reactive agility to a human stimulus.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Oct 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 21, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 28, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 20, 2024
CompletedFirst Submitted
Initial submission to the registry
September 15, 2026
CompletedFirst Posted
Study publicly available on registry
September 28, 2026
CompletedSeptember 28, 2026
September 1, 2026
7 days
September 15, 2026
September 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Planned Agility
The running course was divided into two sections. The first section consisted of a 5 meter linear sprint from a two-point starting position. At the end of the linear section, two cones positioned 1-meter apart marked the change-of-direction area. The participant was instructed by the tester to change the direction of sprinting by cutting at a 45° angle to either the left or right side. The primary outcome measure was the fastest trial completion time, recorded in seconds using a photocell timing system. Timing commenced when the participant crossed the starting gate and ended when the participant crossed the designated gate at the end of course.
40 minutes after caffeine/placebo ingestion
Reactive Agility
The running course was divided into two sections. The first section consisted of a 5 meter linear sprint from a two-point starting position. At the end of the linear section, two cones positioned 1-meter apart marked the change-of-direction area. The participant was instructed by the tester to change the direction of sprinting according to the a) light sensor, b) human movement, by cutting at a 45° angle to either the left or right side. 1. Light sensor showed green arrow of dedicated change-of-direction. This stimulus occured 500 milliseconds after crossing the starting gate. 2. Human tester executed movement to the side when participants were 2.5 meters apart from starting gate. Participants were reacting by the execution of change-of-direction to the opposite side as human tester. The outcome was the fastest completion time, recorded in seconds using a photocell timing system.
45 minutes after caffeine/placebo ingestion
Secondary Outcomes (2)
Countermovement jump
30 minutes after caffeine/placebo ingestion
Drop jump 30
35 minutes after caffeine/placebo ingestion
Study Arms (2)
Caffeine ingestion
EXPERIMENTALSupplementation was administered as caffeine capsules (Scitec Nutrition Caffeine, 100 milligrams per capsule). Participants received 300 mg of caffeine, which represented approximately 3.74 milligrams/kilograms of mean body mass. This dosage corresponded to an individual dose ranging from 3.16 to 4.44 milligrams/kilograms of mean of body mass. The capsules were visually identical, and neither the testers nor the participants were aware of the assigned condition. Caffeine was ingested 30 minutes before the testing session.
Placebo ingestion
PLACEBO COMPARATORSupplementation was administered as a placebo capsules filled with potato starch. The capsules were visually identical, and neither the testers nor the participants were aware of the assigned condition. Placebo pills were ingested 30 minutes before the testing session.
Interventions
Supplementation was administered as caffeine capsules (Scitec Nutrition Caffeine, 100 milligrams per capsule). Subjects received 300 milligrams of caffeine, which represented an individual dose ranging from 3.16 to 4.44 milligrams/kilograms of body mass.
Supplementation was administered as placebo capsules filled with potato starch. The capsules were visually identical, and neither the testers nor the participants were aware of the assigned condition.
Eligibility Criteria
You may qualify if:
- Active male amateur soccer players competing in Slovakian 3rd to 6th tier-league and Austrian 4th to 7th tier-league,
- Regular participation in soccer training and competition,
- No current health restrictions preventing participation in maximal physical testing
- Provided written informed consent
You may not qualify if:
- Goalkeepers
- Current or recent musculoskeletal injury affecting physical performance
- Acute illness at the time of testing
- Cardiovascular or neurological disorders
- Visual impairment affecting performance of the experimental tasks
- Significant sleep disorders
- Habitual caffeine consumption exceeding 400 mg/day
- Failure to complete both experimental sessions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Comenius University in Bratislava, Faculty of Physical Education and Sport
Bratislava, Slovakia, 814 69, Slovakia
Related Publications (5)
Redondo B, Jimenez R, Molina R, Dalton K, Vera J. Effects of caffeine ingestion on dynamic visual acuity: a placebo-controlled, double-blind, balanced-crossover study in low caffeine consumers. Psychopharmacology (Berl). 2021 Dec;238(12):3391-3398. doi: 10.1007/s00213-021-05953-1. Epub 2021 Aug 22.
PMID: 34420061BACKGROUNDGrgic J. Exploring the minimum ergogenic dose of caffeine on resistance exercise performance: A meta-analytic approach. Nutrition. 2022 May;97:111604. doi: 10.1016/j.nut.2022.111604. Epub 2022 Jan 22.
PMID: 35203046BACKGROUNDMerino Fernandez M, Ruiz-Moreno C, Giraldez-Costas V, Gonzalez-Millan C, Matos-Duarte M, Gutierrez-Hellin J, Gonzalez-Garcia J. Caffeine Doses of 3 mg/kg Increase Unilateral and Bilateral Vertical Jump Outcomes in Elite Traditional Jiu-Jitsu Athletes. Nutrients. 2021 May 18;13(5):1705. doi: 10.3390/nu13051705.
PMID: 34069892BACKGROUNDEllis M, Noon M, Myers T, Clarke N. Low Doses of Caffeine: Enhancement of Physical Performance in Elite Adolescent Male Soccer Players. Int J Sports Physiol Perform. 2019 May 1;14(5):569-575. doi: 10.1123/ijspp.2018-0536. Epub 2019 Apr 21.
PMID: 30300047BACKGROUNDStojanovic E, Scanlan AT, Milanovic Z, Fox JL, Stankovic R, Dalbo VJ. Acute caffeine supplementation improves jumping, sprinting, and change-of-direction performance in basketball players when ingested in the morning but not evening. Eur J Sport Sci. 2022 Mar;22(3):360-370. doi: 10.1080/17461391.2021.1874059. Epub 2021 Feb 2.
PMID: 33413049BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Filip Skala, PhD.
Comenius University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant
Study Record Dates
First Submitted
September 15, 2026
First Posted
September 28, 2026
Study Start
October 21, 2024
Primary Completion
October 28, 2024
Study Completion
December 20, 2024
Last Updated
September 28, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share