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Multi-Ingredient Supplementation in Professional Football Players

Dose-Dependent Effects of Multi-Ingredient Supplementation on Physical Performance, Recovery, and Cognitive Function in Professional Football Players

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07604519
Acronym
TCP-Soccer
Enrollment
97
Registered
2026-05-22
Start date
2026-06-14
Completion date
2026-06-30
Last updated
2026-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Performance During Physical Activity, Fatigue, Football Players, Recovery, Sports Performance

Keywords

Soccer, Football, Supplementation, Exercise Performance, Recovery

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.

Detailed description

The planned study will be a randomized, double-blind, placebo-controlled trial designed as a continuation and extension of previous research on multi-ingredient supplementation in professional football players. The primary aim will be to investigate the dose-dependent effects of phosphatidylserine combined with taurine and caffeine under standardized football-specific training conditions and acute cognitive-fatigue conditions. Approximately 80 professional male football players competing at national level will be randomly assigned to four groups: placebo, taurine + caffeine, taurine + caffeine + phosphatidylserine 300 mg, and taurine + caffeine + phosphatidylserine 600 mg. Importantly, caffeine and taurine doses will remain identical across all active supplementation groups in order to enable a more precise evaluation of the independent effects of phosphatidylserine. Participants will complete a 14-day supplementation protocol and undergo baseline and post-intervention assessments including 30 m sprint performance, reaction time, cognitive-fatigue responses, football-specific GPS monitoring, fatigue-related performance decline, recovery-related variables, sleep monitoring, and autonomic nervous system activity assessment. The study is expected to provide novel insights into the role of phosphatidylserine in football-specific performance, cognitive fatigue resistance, recovery, and neurophysiological responses in elite football players.

Interventions

OTHERPlacebo

Placebo capsules administered daily during the 14-day intervention period

DIETARY_SUPPLEMENTtaurine

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

DIETARY_SUPPLEMENTCaffeine

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

DIETARY_SUPPLEMENTPhosphatidylserine

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

Sponsors

Vizja University in Warsaw
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Intervention model description

Participants will be randomly assigned to parallel study groups receiving either placebo or multi-ingredient supplementation during the intervention period.

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

\- Inclusion Criteria: * 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
30 m sprint timeBaseline and after 14 days of supplementationTime 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

Secondary

MeasureTime frameDescription
Relative distanceAfter 14 days of supplementation, during the standardized football-specific training sessionDistance covered per minute during the standardized football-specific training session, measured using a 10-Hz GPS tracking system. Unit of Measure: meters per minute
High-speed running distanceAfter 14 days of supplementation, during the standardized football-specific training sessionDescription: Distance covered at running speeds above 19.8 km/h during the standardized football-specific training session, measured using a 10-Hz GPS tracking system. Unit of Measure: meters
Number of sprintsAfter 14 days of supplementation, during the standardized football-specific training sessionTotal number of sprint efforts performed during the standardized football-specific training session. Sprinting will be defined as running speed above 25.0 km/h and measured using a 10-Hz GPS tracking system. Unit of Measure: number of sprints
Player LoadAfter 14 days of supplementation, during the standardized football-specific training sessionExternal training load during the standardized football-specific training session, measured using triaxial accelerometry integrated with the GPS tracking system. Unit of Measure: arbitrary units
Heart rate variability RMSSDDaily during the 14-day supplementation periodResting heart rate variability assessed in the morning using the root mean square of successive differences between normal heartbeats. HRV will be measured using a heart rate sensor or wearable device under standardized resting conditions. Unit of Measure: milliseconds
Sleep durationDaily during the 14-day supplementation periodTotal sleep duration assessed using wearable sleep monitoring. Unit of Measure: hours
Sleep efficiencyDaily during the 14-day supplementation periodPercentage of time in bed spent asleep, assessed using wearable sleep monitoring. Unit of Measure: percent
Subjective fatigueDaily during the 14-day supplementation periodSubjective fatigue assessed using the fatigue item of the Hooper Index questionnaire on a 1-7 scale, where higher values indicate greater fatigue. Unit of Measure: score on a scale
Muscle sorenessDaily during the 14-day supplementation periodPerceived lower-limb muscle soreness assessed using a 0-10 delayed onset muscle soreness scale, where higher values indicate greater soreness. Unit of Measure: score on a scale
Stroop task reaction timeBaseline and after 14 days of supplementationMean response time during a modified computerized Stroop task assessing cognitive fatigue, inhibitory control, sustained attention, and information processing speed. Unit of Measure: seconds
Stroop task accuracyBaseline and after 14 days of supplementationPercentage of correct responses during a modified computerized Stroop task. Unit of Measure: percent
Stroop task error rateBaseline and after 14 days of supplementationNumber of incorrect responses during a modified computerized Stroop task. Unit of Measure: number of errors
Perceived mental fatigueBaseline and after 14 days of supplementationSubjective perceived mental fatigue assessed using a 0-10 visual analogue scale, where higher values indicate greater perceived mental fatigue. Unit of Measure: score on a 0-10 scale
Change in sprint count between first and second halfAfter 14 days of supplementation, during the standardized football-specific training sessionPercentage decline in the number of sprints between the first and second half of the standardized football-specific training session. Sprint change will be calculated as: \[(second half value - first half value) / first half value\] × 100. Unit of Measure: percent
Visual reaction timeBaseline and after 14 days of supplementationMean response time to a visual stimulus, measured using a validated visual reaction time test.
Total distance coveredAfter 14 days of supplementation, during the standardized football-specific training sessionTotal distance covered during the standardized football-specific training session, measured using a 10-Hz GPS tracking system. Unit of Measure: meters
Auditory reaction timeBaseline and after 14 days of supplementationMean response time to an auditory stimulus, measured using a computerized auditory reaction time test.

Countries

Hungary, Poland, Spain

Contacts

PRINCIPAL_INVESTIGATORKrzysztof Maciej MIZERA, PhD

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 3, 2026