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Clinical Trials in Spain / NCT07402902
Enrolling by invitation Not applicable

Caffeine Strategies and Fat Oxidation

NCT07402902 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-03-15
Last updated
2026-04-29

Condition(s) studied

Fat MetabolismCaffeineCyclingExerciseErgogenics

Investigational drug(s) / intervention(s)

Caffeine (Guinama Anhydrous Powder) →Caffeine (Nescafé Classic Coffee)Caffeine (Kafewake Gum)Caffeine Mouth Rinse SolutionPlacebo (Cellulose Capsule)Placebo (Decaffeinated Coffee)Placebo (Non-caffeine Gum)Placebo Mouth Rinse Solution

Caffeine (Guinama Anhydrous Powder): 3 mg/kg of anhydrous caffeine powder (Guinama, Spain) administered in an opaque capsule 60 min before exercise.

Caffeine (Nescafé Classic Coffee): 3 mg/kg of caffeine via Nescafé Classic (Nestlé, Switzerland) dissolved in 250 mL of water 60 min before exercise.

Caffeine (Kafewake Gum): 3 mg/kg of caffeine via Kafewake gum (Arafarma group, Spain), chewed for 10 min before exercise.

Caffeine Mouth Rinse Solution: 3 mg/kg of caffeine (Nescafé Classic) dissolved in 25 mL of water for a 20-second rinse before exercise.

Placebo (Cellulose Capsule): Opaque capsule containing cellulose powder, matching caffeine capsules, taken 60 min before exercise.

Placebo (Decaffeinated Coffee): Decaffeinated Nescafé (Nestlé, Switzerland) in 250 mL of water, matching caffeinated coffee, taken 60 min before.

Placebo (Non-caffeine Gum): Kafewake Non-caffeinated gum (Arafarma group, Spain) with identical taste and texture, chewed for 10 min before.

Placebo Mouth Rinse Solution: Decaffeinated Nescafé in 25 mL of water for a 20-second rinse immediately before exercise.

Study summary

The goal of this clinical trial is to learn if different forms of caffeine ingestion can influence fat oxidation during submaximal cycling exercise. The study will recruit healthy adults, both men and women, aged 18 to 50, who regularly perform aerobic exercise. The main questions it aims to answer are:

* Does caffeine increase fat oxidation during one hour of cycling at the Fatmax intensity?
* Do different forms of caffeine ingestion (capsule, coffee, chewing gum, or mouth rinse) differ in their effect on fat oxidation?
* Do these caffeine forms alter total energy expenditure, cardiorespiratory response, or perceived exertion during exercise?
* Are there differences in the occurrence or severity of side effects between caffeine administration methods?

Researchers will compare each caffeine form to its corresponding placebo to determine their effects on fat oxidation and other physiological outcomes.

Participants will:

* Attend a pre-experimental session to determine their Fatmax intensity and VO₂max using an incremental cycling test
* Perform eight experimental sessions, each consisting of one hour of cycling at Fatmax intensity
* Receive caffeine or placebo via capsules, coffee, chewing gum, or mouth rinse according to a randomized, double-blind, crossover design
* Be monitored for fat and carbohydrate oxidation, total energy expenditure, heart rate, and perceived exertion during exercise
* Report any side effects immediately after the session and 24 hours later using a structured questionnaire

All sessions will be conducted under controlled laboratory conditions with standardized protocols to ensure safety and reliable measurements.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy men and women aged 18-50 years * Regular aerobic exercise at least 1 hour per day, 2 days per week * Provide written informed consent Exclusion Criteria: * Smoking * Use of medication or ergogenic supplements during the study period * Caffeine intolerance or allergy * Cardiopulmonary or musculoskeletal disorders * Use of oral contraceptives in female participants

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Estadio Raúl González Blanco, Camino del Molino 5 Fuenlabrada Madrid

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07402902 on ClinicalTrials.gov ↗ ← All trials in Spain