Multi-Ingredient Supplementation in Professional Football Players
TCP-Soccer
Dose-Dependent Effects of Multi-Ingredient Supplementation on Physical Performance, Recovery, and Cognitive Function in Professional Football Players
1 other identifier
interventional
100
3 countries
5
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jun 2026
Shorter than P25 for not_applicable
5 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
May 13, 2026
CompletedFirst Posted
Study publicly available on registry
May 22, 2026
CompletedStudy Start
First participant enrolled
June 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2026
Study Completion
Last participant's last visit for all outcomes
July 1, 2026
May 22, 2026
May 1, 2026
1 month
May 13, 2026
May 17, 2026
Conditions
Keywords
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 COMPARATORParticipants will receive visually identical placebo capsules for 14 days.
TC
EXPERIMENTALParticipants will receive taurine (1500 mg/day) and caffeine (200 mg/day) supplementation for 14 days.
TCP-300
EXPERIMENTALParticipants will receive taurine (1500 mg/day), caffeine (200 mg/day), and phosphatidylserine (300 mg/day) supplementation for 14 days.
TCP-600
EXPERIMENTALParticipants will receive taurine (1500 mg/day), caffeine (200 mg/day), and phosphatidylserine (600 mg/day) supplementation for 14 days.
Interventions
Taurine supplementation administered daily during the 14-day intervention period.
Caffeine supplementation administered daily during the 14-day intervention period.
Phosphatidylserine supplementation administered daily during the 14-day intervention period.
Eligibility Criteria
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
Professional Football Training Center
Lodz, Poland
Professional Football Training Center
Warsaw, Poland
Professional Football Training Center
Wroclaw, Poland
Professional Football Training Center
Alicante, Spain
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
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
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- 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