NCT07696052

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
65

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

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

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 10, 2026

Completed
27 days until next milestone

Study Start

First participant enrolled

August 6, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 8, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 8, 2026

Completed
Last Updated

September 14, 2026

Status Verified

September 1, 2026

Enrollment Period

1 month

First QC Date

July 5, 2026

Last Update Submit

September 9, 2026

Conditions

Keywords

PhosphatidylserineTaurineCaffeineFootball PlayersSoccerNeurocognitive LoadVisual SearchEye TrackingTactical Decision-MakingStroop Flanker TaskReactive Passing Decision TestSports Nutrition

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 COMPARATOR

Participants 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.

Dietary Supplement: Placebo

Taurine Plus Caffeine

ACTIVE COMPARATOR

Participants 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.

Dietary Supplement: Taurine Plus Caffeine

Taurine, Caffeine, and Phosphatidylserine

EXPERIMENTAL

Participants 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.

Dietary Supplement: Taurine, Caffeine, and Phosphatidylserine

Interventions

PlaceboDIETARY_SUPPLEMENT

Inert placebo matched with the active supplements for appearance, number of units, and packaging. The placebo will be administered for 28 days.

Placebo
Taurine Plus CaffeineDIETARY_SUPPLEMENT

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 Plus Caffeine

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.

Taurine, Caffeine, and Phosphatidylserine

Eligibility Criteria

Age18 Years - 37 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Location

Professional Football Training Center

Warsaw, Poland

Location

MeSH Terms

Conditions

Mental Fatigue

Interventions

TaurineCaffeinePhosphatidylserines

Condition Hierarchy (Ancestors)

FatigueSigns and SymptomsPathological Conditions, Signs and SymptomsBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Alkanesulfonic AcidsAlkanesHydrocarbons, AcyclicHydrocarbonsOrganic ChemicalsSulfonic AcidsSulfur AcidsSulfur CompoundsXanthinesAlkaloidsHeterocyclic CompoundsPurinonesPurinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingGlycerophospholipidsPhosphatidic AcidsGlycerophosphatesPhospholipidsMembrane LipidsLipids

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
Model Details: Participants were randomized in a 1:1:1 ratio to one of three parallel groups: placebo, taurine plus caffeine, or taurine plus caffeine plus phosphatidylserine. The intervention lasted 28 days, and outcomes were assessed at baseline and after the supplementation period.
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.

Locations