Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Active Not Recruiting NCT07696052

Phosphatidylserine, Taurine, and Caffeine for Cognitive Fatigue in Professional Football Players

Conditions: Mental Fatigue, Cognitive Performance, Athletic Performance, Soccer Performance, Decision Making

Sex: Male
Ages: 18 Years – 37 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 62
Sponsor: Vizja University in Warsaw

Location: Professional Football Training Center Lodz

Summary

This randomized, double-blind, placebo-controlled, parallel-group trial will evaluate 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-two male outfield football players from two professional clubs will be randomized to placebo, taurine plus caffeine, or taurine plus caffeine plus phosphatidylserine. Neurocognitive fatigue resistance will be evaluated during a standardized high-load Stroop/Flanker task, while football-specific tactical decision-making, visual-search behavior, and field-based reactive decision performance will be assessed at baseline and after 28 days of supplementation.

Eligibility Criteria

Inclusion Criteria: * 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. Exclusion Criteria: * 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.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07696052). StuddyBuddy aggregates publicly available trial information.