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Acute Effects of Caffeine on Repeated Sprint Performance and Energy Distribution

18 mei 2026 bijgewerkt door: Abdulkadir Birol, Trabzon University

Acute Effect of Caffeinated and Decaffeinated Coffee Consumption on Repeated Sprint Performance and Energy Contribution Distribution

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

Studie Overzicht

Gedetailleerde beschrijving

This investigation examined whether acute ingestion of low-dose caffeine delivered through commercially available regular coffee would alter repeated sprint capacity and metabolic energy system dynamics in athletes who compete in combat disciplines. A within-subject, double-blind, placebo-controlled crossover framework was adopted to ensure methodological rigor and minimize order and expectation biases. Eligible participants were physically active male combat sports competitors (n = 15; aged 18-25 years) with a documented competitive history spanning at least five years at the regional and national levels. Volunteers were excluded if they reported recent use of performance-modifying agents, stimulant or psychotropic medications, tobacco products, or any diagnosed condition affecting cardiovascular, metabolic, or musculoskeletal function. To standardize caffeine baseline, all participants were instructed to abstain from caffeinated products for a minimum of two weeks prior to the study onset and throughout the entire data collection period.

Each participant attended the laboratory on four separate occasions. The initial visit served as a familiarization session and included anthropometric assessment. The subsequent three sessions were assigned in a randomized, counterbalanced order, with a minimum 48-hour recovery interval separating each visit. During these sessions, participants received one of three coded supplementation conditions - placebo (decaffeinated coffee), low-dose caffeine (1.5 mg·kg-¹ body mass), or moderate-low-dose caffeine (3 mg·kg-¹ body mass) - each dissolved in 250 mL of hot water and consumed over a 10-minute period. The caffeine content of both the caffeinated and decaffeinated coffee products (Nescafe Gold) was verified by an accredited food analysis laboratory. To maintain identical volume, appearance, and taste across all conditions, decaffeinated and caffeinated coffees were blended in varying proportions for each dose level. Supplementation was administered 60 minutes before the commencement of exercise testing. Performance testing comprised a standardized cycling-based repeated sprint protocol: six 10-second maximal effort sprints, each separated by a 30-second passive recovery period, performed on a mechanically braked cycle ergometer (Monark 894E) with resistance set at 10% of individual body mass. A structured warm-up preceded each testing bout. Primary performance variables derived from sprint testing included peak power output, mean power output, and fatigue index. Perceptual and physiological responses were documented via the Borg rating of perceived exertion scale, peak heart rate, and capillary blood lactate concentration measured at rest and immediately following the final sprint. Breath-by-breath oxygen uptake data were collected continuously using a portable metabolic system (COSMED K5) to facilitate estimation of energy system contributions. The relative and absolute contributions of the phosphocreatine (ATP-PCr), glycolytic, and oxidative metabolic pathways were quantified using established indirect methods. Excess post-exercise oxygen consumption (EPOC) kinetics were modeled with mono-exponential curve fitting to isolate the fast EPOC component, which served as a proxy for PCr resynthesis. Glycolytic contribution was estimated from the net change in blood lactate concentration, applying an established oxygen-equivalent conversion factor. Oxidative metabolism was derived from the net elevation in VO₂ above resting values during exercise. Total energy expenditure was computed as the cumulative sum of all three pathway contributions. To control for dietary and diurnal confounders, participants replicated identical pre-test meal patterns documented during the first testing session, and all laboratory visits were conducted between 08:00 and 11:00 h. Dietary adherence was verified through structured diet logs reviewed by the research team. Data were analyzed using one-way repeated-measures ANOVA with Bonferroni-adjusted pairwise comparisons, and partial eta squared (η²p) was reported as the measure of effect magnitude. The study received full ethical clearance from the Trabzon Eurasia University Ethics Committee and was conducted in accordance with the principles outlined in the Declaration of Helsinki. Informed consent form obtained from all the participants.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

15

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Akçaabat
      • Trabzon, Akçaabat, Turkije (Türkiye), 61300
        • Trabzon University Faculty of Sport Sciences

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen

Accepteert gezonde vrijwilligers

Ja

Beschrijving

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Fundamentele wetenschap
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Crossover-opdracht
  • Masker: Dubbele

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Placebo-vergelijker: Placebo
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.
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.
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).
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).
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.
Experimenteel: Low-Dose Caffeine - 1.5 mg·kg-¹
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.
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.
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).
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).
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.
Experimenteel: Low-Dose Caffeine - 3 mg·kg-¹
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.
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.
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).
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).
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.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Peak Power Output
Tijdsspanne: On 3 testing days with 48-hour interval
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
Tijdsspanne: On 3 testing days with 48-hour interval
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
Tijdsspanne: On 3 testing days with 48-hour interval
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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Total Energy Expenditure
Tijdsspanne: On 3 testing days with 48-hour interval
Computed as the cumulative sum of ATP-PCr, glycolytic, and oxidative pathway contributions, expressed in kilojoules (kJ), using a caloric equivalent of 20.92 kJ per liter of O₂ consumed.
On 3 testing days with 48-hour interval
Energy System - Oxidative Contribution
Tijdsspanne: On 3 testing days with 48-hour interval
Estimated absolute contributions (kJ) of each metabolic pathway. Oxidative contribution calculated as net VO₂ elevation above resting baseline. Breath-by-breath VO₂ data collected continuously via COSMED K5 portable metabolic system.
On 3 testing days with 48-hour interval
Energy System - ATP Contribution
Tijdsspanne: On 3 testing days with 48-hour interval
ATP-PCr contribution derived from the fast component of EPOC kinetics modeled via mono-exponential curve fitting (OriginPro 8.0).
On 3 testing days with 48-hour interval
Energy System - Glycolytic Contribution
Tijdsspanne: On 3 testing days with 48-hour interval
Glycolytic contribution estimated from net blood lactate rise (3 mL O₂·kg-¹ per 1 mmol·L-¹ increase).
On 3 testing days with 48-hour interval
Peak Heart Rate
Tijdsspanne: On 3 testing days with 48-hour interval
Highest recorded heart rate (bpm) during the repeated sprint test.
On 3 testing days with 48-hour interval
Delta Blood Lactate Concentration
Tijdsspanne: On 3 testing days with 48-hour interval
Difference between resting capillary blood lactate (measured after 20-minute passive rest prior to testing) and maximum post-exercise lactate (measured immediately following the final sprint). Expressed in mmol·L-¹.
On 3 testing days with 48-hour interval
Rating of Perceived Exertion
Tijdsspanne: On 3 testing days with 48-hour interval
Subjective effort rating collected using the Borg scale (6-20) following the completion of the repeated sprint protocol.
On 3 testing days with 48-hour interval

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

15 april 2025

Primaire voltooiing (Werkelijk)

30 mei 2025

Studie voltooiing (Werkelijk)

30 mei 2025

Studieregistratiedata

Eerst ingediend

12 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

18 mei 2026

Eerst geplaatst (Werkelijk)

19 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

19 mei 2026

Laatste update ingediend die voldeed aan QC-criteria

18 mei 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • E-69268593-050.04-25025

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

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

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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