AzTrials
AzTrials

Fat MetabolismNCT07402902

Caffeine Strategies and Fat Oxidation

A study testing Caffeine (Guinama Anhydrous Powder), Caffeine (Nescafé Classic Coffee) and Caffeine (Kafewake Gum) in people with Fat Metabolism and Caffeine, run by Universidad Rey Juan Carlos at 1 site in Spain.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
Search all trials

Trial 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. Read more about this study

Who is it for?
Ages 18 to 50 yearsHealthy volunteers can take part
Conditions the study is for
Fat Metabolism, Caffeine, Cycling
What is being tested?
Caffeine (Guinama Anhydrous Powder), Caffeine (Nescafé Classic Coffee) and Caffeine (Kafewake Gum)
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
10 participants
Where
1 siteSpain
Study dates
15 Mar 2026to 30 Sep 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Spain1 site
  • Estadio Raúl González Blanco, Camino del Molino 5

    Fuenlabrada, Madrid, 28942

Other trials in Spain

About this study

Official title: Effects of Different Caffeine Ingestion Forms on Fat Oxidation During Cycle Ergometer Exercise

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?
Read more

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.

Being tested
Caffeine (Guinama Anhydrous Powder), Caffeine (Nescafé Classic Coffee), Caffeine (Kafewake Gum), Caffeine Mouth Rinse Solution, Placebo (Cellulose Capsule)
Medical subject headings
Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Caffeine (Guinama Anhydrous Powder)Drug

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

  • Caffeine (Nescafé Classic Coffee)Dietary supplement

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

  • Caffeine (Kafewake Gum)Dietary supplement

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

  • Caffeine Mouth Rinse SolutionOther

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

  • Placebo (Cellulose Capsule)Other

    Opaque capsule containing cellulose powder, matching caffeine capsules, taken 60 min before exercise.

  • Placebo (Decaffeinated Coffee)Other

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

  • Placebo (Non-caffeine Gum)Other

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

  • Placebo Mouth Rinse SolutionOther

    Decaffeinated Nescafé in 25 mL of water for a 20-second rinse immediately before exercise.

Study groups in NCT07402902
Study groupRoleWhat they receive
Caffeine capsuleExperimentalParticipants will ingest 3 mg/kg of anhydrous caffeine powder in an opaque capsule 60 minutes before performing 60 minutes of cycling on a cycle ergometer at Fatmax intensity.
Receives: Drug: Caffeine (Guinama Anhydrous Powder)
Placebo capsulePlacebo comparatorParticipants will ingest an opaque capsule filled with cellulose (placebo) 60 minutes before performing 60 minutes of cycling on a cycle ergometer at Fatmax intensity.
Receives: Other: Placebo (Cellulose Capsule)
Caffeine coffeeExperimentalParticipants will consume 3 mg/kg of caffeine via soluble coffee (Nescafé Classic) in 250 mL of hot water 60 minutes before performing 60 minutes of cycling on a cycle ergometer at Fatmax intensity.
Receives: Dietary Supplement: Caffeine (Nescafé Classic Coffee)
Placebo coffeePlacebo comparatorParticipants will consume decaffeinated soluble coffee (Nescafé Descafeinado) in 250 mL of hot water 60 minutes before performing 60 minutes of cycling on a cycle ergometer at Fatmax intensity.
Receives: Other: Placebo (Decaffeinated Coffee)
Caffeine chewing gumExperimentalParticipants will chew caffeinated gum (Kafewake) containing 3 mg/kg of caffeine for 10 minutes before performing 60 minutes of cycling on a cycle ergometer at Fatmax intensity.
Receives: Dietary Supplement: Caffeine (Kafewake Gum)
Placebo chewing gumPlacebo comparatorParticipants will chew non-caffeinated gum (Kafewake) with identical flavor and texture for 10 minutes before performing 60 minutes of cycling on a cycle ergometer at Fatmax intensity.
Receives: Other: Placebo (Non-caffeine Gum)
Caffeine mouth rinseExperimentalParticipants will perform a 20-second mouth rinse with 25 mL of water containing 3 mg/kg of caffeine from soluble coffee (Nescafé Classic) before performing 60 minutes of cycling on a cycle ergometer at Fatmax intensity.
Receives: Other: Caffeine Mouth Rinse Solution
Placebo mouth rinsePlacebo comparatorParticipants will perform a 20-second mouth rinse with 25 mL of water containing decaffeinated soluble coffee (Nescafé descafeinado) before performing 60 minutes of cycling on a cycle ergometer at Fatmax intensity.
Receives: Other: Placebo Mouth Rinse Solution

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Rate of fat oxidation during submaximal cycling exercise at Fatmax intensity

    Continuous measurement of fat oxidation using indirect calorimetry during 1-hour cycling at Fatmax intensity. Calculated from respiratory gas exchange (VO₂ and VCO₂) using Frayn's equations. Unit of Measure: grams per minute (g/min).

    Measured: 1 hour per experimental session

Secondary outcomes (8)
  1. Rate of carbohydrate oxidation during submaximal cycling exercise at Fatmax intensity

    Continuous measurement of carbohydrate oxidation using indirect calorimetry during 1-hour cycling at Fatmax intensity. Calculated from respiratory gas exchange (VO₂ and VCO₂) using Frayn's equations. Unit of Measure: grams per minute (g/min).

    Measured: 1 hour per experimental session

  2. Total energy expenditure during exercise

    Estimated from indirect calorimetry data using Brouwer's equation, recorded continuously during 1-hour cycling at Fatmax intensity. Unit of Measure: kilocalories per minute (kcal/min).

    Measured: 1 hour per experimental session

  3. Mean Exercise Heart Rate

    Heart rate monitored continuously via a chest strap (Polar H9, Polar Electro, Findland) during the exercise test. Unit of Measure: beats per minute (bpm).

    Measured: 1 hour per experimental session

  4. Oxygen consumption

    Volume of oxygen consumed during the exercise session measured breath-by-breath via indirect calorimetry using the Ergostik gas analyzer (Geratherm Respiratory GmbH, Germany). Unit of Measure: Liters per minute (L/min).

    Measured: 1 hour per experimental session

  5. Carbon Dioxide Production

    Volume of carbon dioxide produced during the exercise session measured breath-by-breath via indirect calorimetry using the Ergostik gas analyzer (Geratherm Respiratory GmbH, Germany). Unit of Measure: Liters per minute (L/min).

    Measured: 1 hour per experimental session

  6. Blood lactate concentration

    Measured from capillary blood samples taken from the fingertip during exercise to assess metabolic response to different caffeine interventions. Unit of measure: Millimoles per liter (mmol/L).

    Measured: Every 20 minutes during each 1-hour session

  7. Rating of Perceived Exertion (RPE) during exercise

    Assessed using Borg's 6-20 scale; participants report perceived exertion at regular intervals. Unit of Measure: Units on a scale (from 6 to 20).

    Measured: Every 10 minutes during each 1-hour session

  8. Occurrence of caffeine-related side effects

    Structured questionnaire assessing symptoms commonly associated with caffeine intake, such as nervousness, tremors, insomnia, gastrointestinal discomfort, and increased heart rate.

    Measured: Immediately after each session and 24 hours post-exercise

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Feb 2026
  2. Study start15 Mar 2026
  3. Primary completion31 Jul 2026 (estimated)
  4. Study completion30 Sep 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Model description
Participants will undergo all experimental conditions (caffeine via capsule, coffee, chewing gum, and mouth rinse, and their corresponding placebos) in a randomized, double-blind, counterbalanced crossover design.
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
10 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07402902
Sponsor's protocol ID
URJC-CAF-FOX-2026
Status last verified
Feb 2026
First submitted
13 Jan 2026
Last updated
29 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified individual participant data underlying the results reported in publications may be made available upon reasonable request. These data may include anonymized metabolic, ventilatory, cardiovascular and perceptual variables collected during the study (e.g., fat oxidation rate, energy expenditure, VO₂, VCO₂, heart rate, capillary blood lactate concentration, and ratings of perceived exertion). Any data sharing will be subject to ethical approval, compliance with applicable data protection regulations, and approval by the study investigators.

Publications

  • Guest NS, VanDusseldorp TA, Nelson MT, Grgic J, Schoenfeld BJ, Jenkins NDM, Arent SM, Antonio J, Stout JR, Trexler ET, Smith-Ryan AE, Goldstein ER, Kalman DS, Campbell BI. International society of sports nutrition position stand: caffeine and exercise performance. J Int Soc Sports Nutr. 2021 Jan 2;18(1):1. doi: 10.1186/s12970-020-00383-4.

    PubMed 33388079
  • Ruiz-Moreno C, Gutierrez-Hellin J, Amaro-Gahete FJ, Gonzalez-Garcia J, Giraldez-Costas V, Perez-Garcia V, Del Coso J. Caffeine increases whole-body fat oxidation during 1 h of cycling at Fatmax. Eur J Nutr. 2021 Jun;60(4):2077-2085. doi: 10.1007/s00394-020-02393-z. Epub 2020 Oct 6.

    PubMed 33025051

Questions about this trial

What is this clinical trial studying?

A study testing Caffeine (Guinama Anhydrous Powder), Caffeine (Nescafé Classic Coffee) and Caffeine (Kafewake Gum) in people with Fat Metabolism and Caffeine, run by Universidad Rey Juan Carlos at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 29 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Rate of fat oxidation during submaximal cycling exercise at Fatmax intensity (time frame: 1 hour per experimental session). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07402902, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Apr 2026; AzTrials last refreshed its copy on 30 Oct 2026.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in