Phosphatidylserine, Taurine, and Caffeine for Cognitive Fatigue in Professional Football Players
TCPS-Foot
Neurocognitive Fatigue Resistance, Visual Search Efficiency, and Tactical Decision-Making After Phosphatidylserine-Containing Taurine-Caffeine Supplementation in Professional Male Football Players
1 other identifier
interventional
65
1 country
2
Brief Summary
This randomized, double-blind, placebo-controlled, parallel-group trial evaluated neurocognitive fatigue resistance and football-specific decision-making following 28 days of taurine-caffeine supplementation with or without phosphatidylserine in professional male football players. Sixty-five male outfield football players from two professional clubs were randomized to placebo, taurine plus caffeine, or taurine plus caffeine plus phosphatidylserine. Neurocognitive fatigue resistance was evaluated during a standardized high-load Stroop/Flanker task, while football-specific tactical decision-making, visual-search behavior, and field-based reactive decision performance were assessed at baseline and after 28 days of supplementation.
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 Aug 2026
Shorter than P25 for not_applicable
2 active sites
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
First Submitted
Initial submission to the registry
July 5, 2026
CompletedFirst Posted
Study publicly available on registry
July 10, 2026
CompletedStudy Start
First participant enrolled
August 6, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 8, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
September 8, 2026
CompletedSeptember 14, 2026
September 1, 2026
1 month
July 5, 2026
September 9, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Tactical Inhibitory Decision Accuracy Under Neurocognitive Load
Tactical inhibitory decision accuracy will be assessed using football-specific video clips requiring inhibition of an immediately attractive but suboptimal tactical action. Responses will be scored as 1 point for an optimal decision, 0.5 points for an acceptable decision, and 0 points for an incorrect decision. The outcome will be calculated as the mean score across inhibitory tactical clips. The score ranges from 0 to 1, with higher values indicating better tactical inhibitory decision accuracy.
Baseline and 28 days of supplementation
Secondary Outcomes (10)
Overall Football-Specific Optimal Decision Rate
Baseline and 28 days of supplementation
Football-Specific Decision Time
Baseline and 28 days of supplementation
Impulsive Tactical Error Rate
Baseline and 28 days of supplementation
Stroop/Flanker Time-on-Task Reaction-Time Trajectory
Baseline and 28 days of supplementation
Stroop/Flanker Reaction-Time Variability
Baseline and 28 days of supplementation
- +5 more secondary outcomes
Study Arms (3)
Placebo
PLACEBO COMPARATORParticipants randomized to this arm will receive an inert placebo for 28 days. The placebo will be provided in identical coded packs matched for appearance, number of units, and packaging with the active supplements.
Taurine Plus Caffeine
ACTIVE COMPARATORParticipants randomized to this arm will receive taurine 1500 mg/day plus caffeine 200 mg/day for 28 days. On training and testing days, the supplement will be consumed approximately 60 minutes before the main training session or testing procedure. On non-training days, it will be consumed at a consistent morning time.
Taurine, Caffeine, and Phosphatidylserine
EXPERIMENTALParticipants randomized to this arm will receive taurine 1500 mg/day plus caffeine 200 mg/day plus phosphatidylserine 600 mg/day for 28 days. On training and testing days, the supplement will be consumed approximately 60 minutes before the main training session or testing procedure. On non-training days, it will be consumed at a consistent morning time.
Interventions
Inert placebo matched with the active supplements for appearance, number of units, and packaging. The placebo will be administered for 28 days.
Taurine 1500 mg/day plus caffeine 200 mg/day administered for 28 days. On training and testing days, the supplement will be consumed approximately 60 minutes before the main training session or testing procedure. On non-training days, it will be consumed at a consistent morning time.
Taurine 1500 mg/day plus caffeine 200 mg/day plus phosphatidylserine 600 mg/day administered for 28 days. On training and testing days, the supplement will be consumed approximately 60 minutes before the main training session or testing procedure. On non-training days, it will be consumed at a consistent morning time.
Eligibility Criteria
You may qualify if:
- Male professional outfield football players aged 18 to 37 years.
- First-team players or selected U19 players aged 18 years or older who are regularly integrated into first-team training.
- Regular participation in club training.
- At least 5 years of systematic football training experience.
- Free from injury or illness limiting full participation in training and testing.
- Normal or corrected-to-normal vision.
- Ability to complete the laboratory and field-based testing procedures.
- Written informed consent provided before participation.
You may not qualify if:
- Goalkeepers.
- Current injury or illness limiting full participation in testing.
- Neurological disease.
- Recent concussion or head trauma.
- Uncorrected visual impairment.
- Use of phosphatidylserine, nootropic agents, or strong stimulants during the previous 4 weeks.
- Non-standard caffeine intake on testing days.
- Failure to comply with pre-test standardization procedures.
- Failed eye-tracker calibration.
- Loss of more than 30% of gaze data during the football-specific decision-making task.
- Withdrawal of consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Professional Football Training Center
Lodz, Poland
Professional Football Training Center
Warsaw, Poland
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- Participants, investigators, relevant club staff involved in supplementation, and outcome assessors were blinded to treatment allocation. Study products were provided in identically coded packages matched for appearance, number of units, and total mass. The allocation sequence was retained by an independent individual not involved in recruitment, supplementation, outcome assessment, data management, or statistical analysis. Treatment codes were not released until completion of the prespecified primary analysis.
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator and Assistant Professor
Study Record Dates
First Submitted
July 5, 2026
First Posted
July 10, 2026
Study Start
August 6, 2026
Primary Completion
September 8, 2026
Study Completion
September 8, 2026
Last Updated
September 14, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share
No individual participant data will be shared because the study includes a small sample of professional football players from a limited number of clubs, which may increase the risk of indirect participant identification. Only aggregated and anonymized study results will be reported.