NCT07604519

Brief Summary

This randomized double-blind placebo-controlled trial will investigate the effects of multi-ingredient supplementation containing taurine, caffeine, and phosphatidylserine on physical performance, cognitive function, cognitive fatigue responses, recovery, sleep quality, and autonomic nervous system activity in elite male soccer players. Participants will complete a 14-day supplementation protocol and undergo football-specific performance, reaction-time, cognitive-fatigue, recovery, and sleep-related assessments before and after the intervention. The study aims to determine whether phosphatidylserine dose influences physical, cognitive, fatigue-related, and recovery-related outcomes when combined with taurine and caffeine.

Trial Health

67
Monitor

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Jun 2026

Shorter than P25 for not_applicable

Geographic Reach
3 countries

5 active sites

Status
not yet recruiting

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

May 13, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 22, 2026

Completed
10 days until next milestone

Study Start

First participant enrolled

June 1, 2026

Expected
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2026

Last Updated

May 22, 2026

Status Verified

May 1, 2026

Enrollment Period

1 month

First QC Date

May 13, 2026

Last Update Submit

May 17, 2026

Conditions

Keywords

SoccerFootballSupplementationExercise PerformanceRecovery

Outcome Measures

Primary Outcomes (1)

  • 30 m sprint time

    Time required to complete a 30 m sprint, measured using electronic timing gates. The best result from three maximal sprint trials will be used for analysis. Unit of Measure: seconds

    Baseline and after 14 days of supplementation

Secondary Outcomes (17)

  • Fatigue-related sprint decline

    After 14 days of supplementation, during the standardized football-specific training session

  • Visual reaction time

    Baseline and after 14 days of supplementation

  • Auditory reaction time

    Baseline and after 14 days of supplementation

  • Total distance covered

    After 14 days of supplementation, during the standardized football-specific training session

  • Relative distance

    After 14 days of supplementation, during the standardized football-specific training session

  • +12 more secondary outcomes

Study Arms (4)

P

PLACEBO COMPARATOR

Participants will receive visually identical placebo capsules for 14 days.

Other: Placebo

TC

EXPERIMENTAL

Participants will receive taurine (1500 mg/day) and caffeine (200 mg/day) supplementation for 14 days.

Dietary Supplement: taurineDietary Supplement: Caffeine

TCP-300

EXPERIMENTAL

Participants will receive taurine (1500 mg/day), caffeine (200 mg/day), and phosphatidylserine (300 mg/day) supplementation for 14 days.

Dietary Supplement: taurineDietary Supplement: CaffeineDietary Supplement: Phosphatidylserine

TCP-600

EXPERIMENTAL

Participants will receive taurine (1500 mg/day), caffeine (200 mg/day), and phosphatidylserine (600 mg/day) supplementation for 14 days.

Dietary Supplement: taurineDietary Supplement: CaffeineDietary Supplement: Phosphatidylserine

Interventions

PlaceboOTHER

Placebo capsules administered daily during the 14-day intervention period

P
taurineDIETARY_SUPPLEMENT

Taurine supplementation administered daily during the 14-day intervention period.

TCTCP-300TCP-600
CaffeineDIETARY_SUPPLEMENT

Caffeine supplementation administered daily during the 14-day intervention period.

TCTCP-300TCP-600
PhosphatidylserineDIETARY_SUPPLEMENT

Phosphatidylserine supplementation administered daily during the 14-day intervention period.

TCP-300TCP-600

Eligibility Criteria

Age18 Years - 35 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Professional male football players aged 18-35 years
  • Regular participation in team training and competitive matches
  • Clinically healthy status confirmed prior to participation
  • Written informed consent provided

You may not qualify if:

  • Current musculoskeletal injury or illness
  • Chronic metabolic, cardiovascular, or neurological disease
  • Regular medication use
  • Current use of dietary supplements or ergogenic aids
  • Smoking or excessive alcohol consumption
  • Known hypersensitivity to any study supplement ingredient

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (5)

Professional Football Training Center

Budapest, Hungary

Location

Professional Football Training Center

Lodz, Poland

Location

Professional Football Training Center

Warsaw, Poland

Location

Professional Football Training Center

Wroclaw, Poland

Location

Professional Football Training Center

Alicante, Spain

Location

MeSH Terms

Conditions

Fatigue

Interventions

TaurineCaffeinePhosphatidylserines

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

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

Study Officials

  • Krzysztof Maciej MIZERA, PhD

    1. Vizja University in Warsaw, Faculty of Medical Sciences and Health Sciences, 01-143 Warsaw, Poland

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Krzysztof Maciej Mizera, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to parallel study groups receiving either placebo or multi-ingredient supplementation during the intervention period.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 13, 2026

First Posted

May 22, 2026

Study Start (Estimated)

June 1, 2026

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

July 1, 2026

Last Updated

May 22, 2026

Record last verified: 2026-05

Locations