NCT07596511

Brief Summary

The goal of this study is to learn if low-dose caffeinated coffee improves repeated sprint performance and affects energy system contributions in combat sports athletes. The main questions it aims to answer are:

  • Does low-dose caffeinated coffee (1.5 or 3 mg·kg-¹) improve peak power, mean power, and fatigue index during repeated sprint tests?
  • What physiological responses (heart rate, blood lactate, perceived exertion, and energy system contributions) do participants have when consuming caffeinated coffee? Researchers compared caffeinated coffee at two doses (1.5 and 3 mg·kg-¹ body mass) to a placebo (decaffeinated coffee of identical taste and appearance) to see if low

Trial Health

87
On Track

Trial Health Score

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

Enrollment
15

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

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

Study Start

First participant enrolled

April 15, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 30, 2025

Completed
12 months until next milestone

First Submitted

Initial submission to the registry

May 12, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 19, 2026

Completed
Last Updated

May 19, 2026

Status Verified

May 1, 2026

Enrollment Period

2 months

First QC Date

May 12, 2026

Last Update Submit

May 18, 2026

Conditions

Keywords

basic science

Outcome Measures

Primary Outcomes (3)

  • Peak Power Output

    Highest instantaneous power output (Watts) recorded across all six 10-second sprint bouts on the cycle ergometer (Monark 894E), with resistance set at 10% of body mass.

    On 3 testing days with 48-hour interval

  • Mean Power Output

    Average power output (Watts) calculated across all six sprint efforts, reflecting the athlete's overall capacity to sustain high-intensity output across the full protocol.

    On 3 testing days with 48-hour interval

  • Fatigue Index

    Quantified as: FI = 100 × (1 - total peak power / ideal peak power), where ideal peak power is the product of the highest single-sprint peak power and the total number of repetitions. Expressed as a percentage (%).

    On 3 testing days with 48-hour interval

Secondary Outcomes (7)

  • Total Energy Expenditure

    On 3 testing days with 48-hour interval

  • Energy System - Oxidative Contribution

    On 3 testing days with 48-hour interval

  • Energy System - ATP Contribution

    On 3 testing days with 48-hour interval

  • Energy System - Glycolytic Contribution

    On 3 testing days with 48-hour interval

  • Peak Heart Rate

    On 3 testing days with 48-hour interval

  • +2 more secondary outcomes

Study Arms (3)

Placebo

PLACEBO COMPARATOR

Participants ingested decaffeinated coffee (Nescafe Gold, decaffeinated) at a dose equivalent to 3 mg·kg-¹ of body mass, dissolved in 250 mL of hot water and consumed over 10 minutes, administered 60 minutes before the exercise test.

Other: Cycling Repeated Sprint Test (6 × 10 s)Other: Breath-by-Breath VO₂ Monitoring - COSMED K5Other: Capillary Blood Lactate Sampling (non-invasive)Other: Heart Rate Monitoring

Low-Dose Caffeine - 1.5 mg·kg-¹

EXPERIMENTAL

A blended preparation of caffeinated and decaffeinated (for the similar taste of intensity with 3 mg/kg intervention) Nescafe Gold coffee dissolved in 250 ml hot water was administered at a total dose corresponding to 1.5 mg·kg-¹ body mass of caffeine. Volume was equalized to the placebo condition through addition of decaffeinated coffee.

Other: Cycling Repeated Sprint Test (6 × 10 s)Other: Breath-by-Breath VO₂ Monitoring - COSMED K5Other: Capillary Blood Lactate Sampling (non-invasive)Other: Heart Rate Monitoring

Low-Dose Caffeine - 3 mg·kg-¹

EXPERIMENTAL

Regular caffeinated Nescafe Gold coffee dissolved in 250 ml hot water was administered at a dose delivering 3 mg·kg-¹ body mass of caffeine.

Other: Cycling Repeated Sprint Test (6 × 10 s)Other: Breath-by-Breath VO₂ Monitoring - COSMED K5Other: Capillary Blood Lactate Sampling (non-invasive)Other: Heart Rate Monitoring

Interventions

A standardized cycling-based repeated sprint protocol consisting of six 10-second maximal-effort sprints, each separated by a 30-second passive rest interval, performed on a mechanically braked cycle ergometer (Monark 894E, Vansbro, Sweden). Resistance was calibrated at 10% of the participant's individual body mass. The inertial momentum of the flywheel was excluded from power output calculations following the approach described by Bogdanis et al. (2008). Each session was preceded by a structured warm-up consisting of five 30-second bouts at 100 W, followed by a 5-minute seated rest before test commencement. Each participant initiated the protocol with their dominant leg to ensure procedural consistency across all sessions.

Low-Dose Caffeine - 1.5 mg·kg-¹Low-Dose Caffeine - 3 mg·kg-¹Placebo

Continuous breath-by-breath oxygen uptake (VO₂) data were collected throughout each testing session using the COSMED K5 portable metabolic system (Rome, Italy). Data were used to estimate the relative and absolute contributions of the three metabolic energy pathways. The fast component of excess post-exercise oxygen consumption (EPOC) was extracted and modeled using a mono-exponential function (OriginPro 8.0, OriginLab Corp.) to estimate phosphocreatine (PCr) resynthesis during recovery intervals and following the final sprint. Oxidative metabolism contribution was derived by subtracting resting VO₂ from exercise VO₂. Total energy demand was expressed in both liters of O₂ and kilojoules (caloric equivalent: 20.92 kJ·L-¹ O₂).

Low-Dose Caffeine - 1.5 mg·kg-¹Low-Dose Caffeine - 3 mg·kg-¹Placebo

Capillary blood samples were obtained at two time points per session: (1) resting lactate (LA\_rest) - collected following a 20-minute passive rest period immediately before the sprint test, in accordance with published lactate clearance protocols; and (2) maximal post-exercise lactate (LA\_max) - collected immediately upon completion of the final sprint repetition. Delta lactate (ΔLA) was calculated as the arithmetic difference between LA\_max and LA\_rest and expressed in mmol·L-¹. Delta lactate values were additionally used to estimate the glycolytic energy system contribution, applying a conversion factor of 3 mL O₂·kg-¹ body mass per 1 mmol·L-¹ increase in blood lactate concentration (Di Prampero \& Ferretti, 1999).

Low-Dose Caffeine - 1.5 mg·kg-¹Low-Dose Caffeine - 3 mg·kg-¹Placebo

Continuous heart rate was recorded throughout each testing session via chest type radiotelemetry sensor integrated with COSMED K5. Peak heart rate (HR\_peak, bpm) was defined as the highest value observed across the entire repeated sprint protocol and reported as a secondary physiological outcome.

Low-Dose Caffeine - 1.5 mg·kg-¹Low-Dose Caffeine - 3 mg·kg-¹Placebo

Eligibility Criteria

Age18 Years - 25 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Male combat sports athletes aged 18 to 25 years
  • Minimum of five years of continuous structured training
  • Competitive experience at both regional (state) and national levels
  • Willingness to abstain from all caffeinated products for two weeks prior to and throughout the study period
  • Ability to follow a standardized dietary protocol prescribed by an Olympic Preparation Center dietitian
  • Provision of written informed consent

You may not qualify if:

  • Age below 18 years
  • Self-reported use of anabolic agents, hormonal modulators, or performance-influencing dietary supplements within the three months preceding enrollment
  • Current use of narcotic, psychotropic, stimulant medications, or tobacco products during the assessment period
  • Presence of any diagnosed medical condition (including cardiovascular, metabolic, neurological, respiratory, or musculoskeletal disorders) that may compromise safe participation
  • Withdrawal from the study at the participant's own request

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Trabzon University Faculty of Sport Sciences

Trabzon, Akçaabat, 61300, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assisstant Professor - PHD

Study Record Dates

First Submitted

May 12, 2026

First Posted

May 19, 2026

Study Start

April 15, 2025

Primary Completion

May 30, 2025

Study Completion

May 30, 2025

Last Updated

May 19, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

All the data collected in this study anonymized and only will be used in the scope of academic paper publication.

Locations