NCT07497685

Brief Summary

This study investigated the effects of different caffeine delivery forms on aerobic and anaerobic exercise performance in healthy adults. Participants completed experimental trials involving caffeine capsule ingestion, caffeine gum chewing, and caffeine mouth rinse conditions. Aerobic performance was assessed using maximal oxygen uptake (VO2max), and anaerobic performance was evaluated using the Wingate anaerobic test. The study used a randomized crossover design where each participant completed all experimental conditions.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
14

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2024

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

October 10, 2024

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 10, 2024

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 10, 2025

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

March 23, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

March 27, 2026

Completed
Last Updated

March 27, 2026

Status Verified

March 1, 2026

Enrollment Period

1 month

First QC Date

March 23, 2026

Last Update Submit

March 23, 2026

Conditions

Keywords

Caffeine Aerobic Performance Anaerobic Performance VO2max Wingate Test Ergogenic Aid Exercise Physiology

Outcome Measures

Primary Outcomes (3)

  • Aerobic Capacity (VO2max)

    Description: Estimated maximal oxygen uptake calculated via the 20-meter shuttle run test (Beep Test).Metric: Milliliters per kilogram per minute (ml/kg/min)

    Measured after each 48-hour washout period following the specific caffeine or placebo intervention

  • Aerobic Capacity (VO2max)

    Estimated maximal oxygen uptake calculated via the 20-meter shuttle run test (Beep Test).

    Measured after each 48-hour washout period following the specific caffeine or placebo intervention

  • Anaerobic Average Power

    The mean power output maintained over the duration of a 30-second Wingate Anaerobic Test

    Measured after each 48-hour washout period following the specific caffeine or placebo intervention.

Study Arms (3)

Caffeine Capsule

EXPERIMENTAL

Participants ingest 300 mg of anhydrous caffeine in tablet form with 100 mL of water exactly 60 minutes prior to exercise. This timing is selected to allow for gastrointestinal absorption and to reach peak plasma concentration.

Other: Comparative Acute Effects of Caffeine Delivery Forms (Capsule, Chewing Gum, Mouth Rinse) on Aerobic Capacity and Wingate Anaerobic Performance Outcomes in Recreational Male Athletes: A Randomized Coun

Caffeine Gum

EXPERIMENTAL

Participants chew caffeinated gum (containing 300 mg of caffeine) for 5 minutes, finishing just before the exercises begin. This method utilizes rapid transmucosal absorption through the oral mucosa to potentially bypass first-pass metabolism.

Other: Comparative Acute Effects of Caffeine Delivery Forms (Capsule, Chewing Gum, Mouth Rinse) on Aerobic Capacity and Wingate Anaerobic Performance Outcomes in Recreational Male Athletes: A Randomized Coun

Caffeine Mouth Rinse

EXPERIMENTAL

Participants rinse with 25 mL of a 1.2% caffeine solution (containing 300 mg of caffeine) for 10 seconds immediately before the exercises and then expectorate the solution completely. Swallowing is strictly prohibited to ensure the effect is triggered primarily through oropharyngeal receptors rather than systemic absorption.

Other: Comparative Acute Effects of Caffeine Delivery Forms (Capsule, Chewing Gum, Mouth Rinse) on Aerobic Capacity and Wingate Anaerobic Performance Outcomes in Recreational Male Athletes: A Randomized Coun

Interventions

This study evaluates the acute effects of three distinct caffeine delivery methods compared to a placebo, using a standardized total dose of 300 mg of caffeine across all active interventions. The study is a randomized, single-blind, counterbalanced crossover trial involving 14 recreational male athletes. The interventions are distinguished by their specific absorption kinetics and ecologically valid administration timings

Caffeine CapsuleCaffeine GumCaffeine Mouth Rinse

Eligibility Criteria

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

You may qualify if:

  • Being a healthy male recreational athlete between the ages of 18-25.
  • Having at least 2 years of regular training history (3-4 days per week).
  • Being a non-smoker and having no chronic diseases or musculoskeletal injuries.
  • Willingness to abstain from caffeine, alcohol, and strenuous exercise 48 hours before each test session.

You may not qualify if:

  • Having a known allergy or sensitivity to caffeine.
  • Using any other performance-enhancing supplements during the study period.
  • Failure to adhere to the standardized nutritional or sleep requirements before testing.
  • Inability to complete all four experimental trials (Capsule, Gum, Rinse, Placebo).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Gaziantep University, Faculty of Sport Science (Athletic Performance Laboratory)

Şehitkamil, Gaziantep, 27310, Turkey (Türkiye)

Location

Related Publications (10)

  • https://doi.org/10.5812/asjsm.34607

    BACKGROUND
  • https://doi.org/10.1007/s40279-017-0776-1

    BACKGROUND
  • https://doi.org/10.1080/17461391.2019.1601261

    BACKGROUND
  • https://doi.org/10.1007/s40279-014-0257-8

    BACKGROUND
  • https://doi.org/10.1136/bjsports-2018-100278

    BACKGROUND
  • https://doi.org/10.3390/medicina57010008

    BACKGROUND
  • https://doi.org/10.1007/s40279-017-0848-2

    BACKGROUND
  • https://doi.org/10.1186/s12970-020-00383-4

    BACKGROUND
  • https://doi.org/10.2478/hukin-2021-0070

    BACKGROUND
  • https://doi.org/10.23751/pn.v25i3.14659

    BACKGROUND

MeSH Terms

Interventions

CapsulesChewing GumMouthwashes

Intervention Hierarchy (Ancestors)

Dosage FormsPharmaceutical PreparationsPlant GumsBiopolymersPolymersMacromolecular SubstancesPolysaccharidesCarbohydratesPlant ExudatesBiological ProductsComplex MixturesCandyFoodDiet, Food, and NutritionPhysiological PhenomenaFood and BeveragesBiomedical and Dental MaterialsSpecialty Uses of ChemicalsChemical Actions and UsesCosmeticsManufactured MaterialsTechnology, Industry, and Agriculture

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
CROSSOVER
Model Details: Participants completed all experimental conditions in a randomized crossover order. Each participant performed exercise tests under three different caffeine administration conditions (caffeine capsule, caffeine gum, and caffeine mouth rinse). The order of the conditions was randomized, and adequate washout periods were provided between trials to minimize carryover effects.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Researcher

Study Record Dates

First Submitted

March 23, 2026

First Posted

March 27, 2026

Study Start

October 10, 2024

Primary Completion

November 10, 2024

Study Completion

March 10, 2025

Last Updated

March 27, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will share

The individual participant data that underlie the results reported in this article, after de-identification (text, tables, figures, and appendices), will be made available to researchers who provide a methodologically sound proposal. Data will be available beginning 6 months and ending 36 months following publication. Requests should be directed to mehmetvrl27@hotmail.com. To gain access, data requestors will need to sign a data access agreement.

Shared Documents
STUDY PROTOCOL, SAP, CSR

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