Effects of Supplementation on Performance in Football Players
FOOTBALL-TCP
Effects of Combined Taurine, Caffeine, and Phosphatidylserine Supplementation on Physical and Cognitive Performance in Professional Male Football Players
1 other identifier
interventional
81
1 country
1
Brief Summary
This study investigated the effects of short-term supplementation with taurine, caffeine, and phosphatidylserine on physical and cognitive performance in professional male football players. Eighty-one players were randomly assigned to one of three groups: placebo, taurine plus caffeine, or taurine plus caffeine combined with phosphatidylserine. Supplementation was administered for 10 days, with a final dose taken 60 minutes before a standardized 105-minute football training session. Primary and secondary outcomes included sprint performance, reaction time, GPS-derived locomotor variables, and technical and tactical performance indicators. The aim of the study was to evaluate whether combined multi-ingredient supplementation could improve performance and attenuate fatigue-related declines under match-like conditions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Mar 2025
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
March 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 5, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 5, 2025
CompletedFirst Submitted
Initial submission to the registry
April 28, 2026
CompletedFirst Posted
Study publicly available on registry
May 12, 2026
CompletedMay 12, 2026
May 1, 2026
11 days
April 28, 2026
May 5, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
30 m sprint time (seconds)
Time to complete a 30 meter sprint under standardized conditions, expressed in seconds; calculated as the mean of valid trials.
Day 10 (final training session following supplementation)
Secondary Outcomes (5)
Reaction time (visual and auditory)
Day 10 (post-supplementation)
Total distance (meters)
Day 10 (during standardized training session)
Running speed (m/s)
Day 10 (during standardized training session)
Sprint count (number)
Day 10 (during standardized training session)
High-speed running distance (meters)
Day 10 (during standardized training session)
Other Outcomes (6)
Sprint time decline (%)
Day 10 (during final training session; comparison between first and second halves)
Running speed decline (%)
Day 10 (during final training session; comparison between first and second halves)
Passing accuracy (%)
Day 10 (during standardized training session)
- +3 more other outcomes
Study Arms (3)
Placebo
PLACEBO COMPARATORParticipants received a placebo (lactose) daily for 10 days.
Taurine + Caffeine
EXPERIMENTALParticipants received taurine (1500 mg) and caffeine (200 mg) daily for 10 days.
Taurine + Caffeine + PS
EXPERIMENTALParticipants received taurine (1500 mg), caffeine (150 mg), and phosphatidylserine (300 mg) daily for 10 days.
Interventions
Taurine 1500 mg and caffeine 200 mg administered daily for 10 days
Taurine 1500 mg, caffeine 150 mg, and phosphatidylserine 300 mg administered daily for 10 days
Eligibility Criteria
You may qualify if:
- Male professional football (soccer) players
- Age 19-32 years
- Currently participating in regular team training (4-5 sessions per week)
- Medically cleared for participation in high-intensity physical activity
- Provided written informed consent
You may not qualify if:
- Current injury or musculoskeletal condition affecting performance
- Chronic disease or medical condition
- Use of medications that may affect physical or cognitive performance
- Regular use of dietary supplements or caffeine prior to the study period
- Smoking or alcohol consumption
- Failure to comply with study procedures
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Krzysztof Mizeralead
Study Sites (1)
ŁKS Łódź
Lodz, Łódżkie, 94-020, Poland
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Krzysztof Maciej MIZERA, PhD
1. Vizja University in Warsaw, Faculty of Medical Sciences and Health Sciences, 01-143 Warsaw, Poland
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, CARE PROVIDER
- Masking Details
- Participants were blinded to group allocation. Supplements and placebo were identical in appearance. Investigators were aware of group assignments.
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 28, 2026
First Posted
May 12, 2026
Study Start
March 25, 2025
Primary Completion
April 5, 2025
Study Completion
April 5, 2025
Last Updated
May 12, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be publicly available due to confidentiality restrictions related to professional athletes. Data may be available from the corresponding author upon reasonable request.