CClinicalTrials.gg
CompletedNCT06891469Updated Mar 26, 2025

Effects of an Acute Dose of Caffeine on the Performance of CrossFit Athletes

An interventional study of Caffeine administration according to body mass (moderate intake- 7 mg/kg) and Placebo (Biotin Capsules) in Healthy, Young Adults and Athletic Performance, sponsored by Democritus University of Thrace. Completed at 1 site in Greece. Open to male participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2025-03-26.

Sponsored by Democritus University of Thrace · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 3 years 1 month after the study started (first participant enrolled Jan 2022, registered Mar 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Male
01

Study summary

The goal of this clinical trial was to investigate the effect of an acute dose of caffeine on CrossFit performance in young, healthy male CrossFit athletes. The main questions it aimed to answer were whether an acute dose of caffeine, compared to placebo:

  • Can improve performance in a specific CrossFit workout
  • Leads to a reduction in the Rating of Perceived Exertion
  • Leads to an increase in blood lactate concentration at the end of the workout

Participants had to:

  • Complete two sessions of a specific CrossFit training program (four rounds of five exercises, 50 seconds of exercise/10 seconds of rest), 60 minutes after consuming either anhydrous caffeine (7.1 ± 0.7 mg/kg of body mass) or an equivalent amount of placebo, aiming to perform as many repetitions as possible.
  • Report subjective perception of fatigue using the Borg scale at the end of each round.
Read the detailed description

Preliminary measurements The preliminary measurements included anthropometry, body composition estimation, dietary and habitual caffeine consumption assessment. To assess habitual caffeine consumption, the volunteers were asked to answer a questionnaire through an interview, which investigated the typical consumption of specific caffeine-containing foods and beverages over the past month. Additionally, medical history information was collected through personal interviews.

Main tests Aerobic fitness and maximum heart rate were assessed using the 20-meter shuttle run at an indoor gymnasium. For each main session, the volunteers arrived at the gym having followed specific preparation instructions. Specifically, they were instructed to avoid intense exercise for 24 hours before the test, be hydrated, eat a carbohydrate-rich meal 3-4 hours earlier, avoid alcohol for 24 hours before the test, and refrain from energy drinks, supplements, or caffeine on the test day.

The two main tests were conducted at the same time of day and under similar environmental conditions for each volunteer. After being weighed, the volunteers took either caffeine or biotin capsules, and, 40 minutes later, they began warming up so that the training session would start 60 minutes after taking the supplement. Before the warm-up, blood lactate concentration was measured using the Lactate Scout 4 automatic lactate analyzer.

The volunteers executed five exercises (50 seconds on, 10 seconds off) for four rounds, aiming to perform as many repetitions as possible with the correct technique. The five exercises were push-ups, power cleans, front squats, sit-ups, and deadlifts. The power clean, front squat, and deadlift were performed with an external load of approximately 40%, 50%, and 60% of body weight, respectively.

Performance was defined as the total number of repetitions per round (i.e. the sum of repetitions in all exercises per round), as well as the number of repetitions performed in each exercise per round.

At the end of each round, the rating of perceived exertion (RPE) was recorded using the 6-to-20 Borg scale, and, one minute after the end of the workout, blood lactate concentration was measured again.

HR was monitored using a HR monitor (Polar H10) throughout the workout and averaged over each round.

Additionally, after completing the training sessions, the volunteers provided information about possible side effects (tachycardia, palpitations, feelings of anxiety/discomfort, headache, dizziness).

02

Conditions studied

  • Healthy, Young Adults
  • Athletic Performance

Keywords

  • caffeine
  • rating of perceived exertion
  • lactate
  • performance
  • high intensity functional training
  • CrossFit®
03

In context

Lead sponsor

Democritus University of Thrace is the lead sponsor of 70 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • Men
  • Aged 18-40
  • At least 2 years of experience with CrossFit programs
  • Free of any medical condition that prevents the participant from performing the exercises of the training program at maximum capacity

Exclusion criteria

Exclusion Criteria:

  • Consumption of caffeine and guarana supplements, unless were discontinued for at least two weeks before participating in the study
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
12 participants (actual)

Study arms

  • Active comparator
    Caffeine

    Consumption of 7.1 ±0.7 mg/kg of body mass of anhydrous caffeine (Pure Caffeine tablets by Myprotein), 60 minutes before the start of the specific CrossFit training program (four rounds of five exercises, 50 seconds exercise/10 seconds rest)

    Dietary Supplement: Caffeine administration according to body mass (moderate intake- 7 mg/kg)

  • Placebo comparator
    Placebo

    Consumption of biotin (BIOTIN tablets by Myprotein) as placebo, 60 minutes before the start of the specific CrossFit training program (four rounds of five exercises, 50 seconds exercise/10 seconds rest). The volunteers received the same number of capsules that they received in caffeine condition

    Dietary Supplement: Placebo (Biotin Capsules)

Interventions

  • Dietary supplementCaffeine administration according to body mass (moderate intake- 7 mg/kg)

    This randomized, double-blind, crossover study aimed to investigate the acute effects of caffeine consumption on physiological responses and performance during a strength-focused CrossFit workout. Participants will consume either anhydrous caffeine (7.1 ± 0.7 mg/kg of body mass) or placebo, 60 minutes before a CrossFit workout aiming to perform as many repetitions as possible.

  • Dietary supplementPlacebo (Biotin Capsules)

    Consumption of biotin (BIOTIN tablets by Myprotein) at the same time as caffeine.

06

What researchers measure

Primary outcomes

  1. Performance During CrossFit® Workout

    Performance was defined as the total number of repetitions completed by the volunteers in the CrossFit program, the repetitions of all exercises per round, and the repetitions of each specific exercise per round.

    Time frame: After 5, 10, 15 and 20 minutes of exercise

  2. Rating of Perceived Exertion during the CrossFit program

    Each partictipant had to record the subjective perception of fatigue, using the Borg scale (6 to 20, with higher score meaning feeling of higher exertion), at the end of each round of CrossFit program

    Time frame: during the last 10 s of the 5th, 10th, 15th and 20th minute of exercise

  3. Blood lactate concentration

    Blood lactate concentration was measured using the Lactate Scout 4 automatic lactate analyzer (EKF Diagnostics) in two time points: before the warm-up for CrossFit program and one minute after the end of the workout

    Time frame: 1st measurement before the warm up and 2nd measurement one minute after the end of workout (i.e. after 20 min of exercise)

Secondary outcomes

  1. Heart Rate

    Throughout the workout, heart rate was monitored using a heart rate monitor (Polar H10)

    Time frame: Heart rate was measured every 1 second of exercise. For analysis, heart rate was averaged over the following time ranges: 1-5 , 6-10 , 11-15 and 16-20 minutes of exercise

  2. Aerobic fitness assessment

    Maximum oxygen consumption was estimated using the 20-meter shuttle run test from the number of shuttles completed at exhaustion.

    Time frame: baseline (during the 2nd visit)

  3. Maximum heart rate measurement

    Maximum Heart rate was determined during the 20-meter shuttle run test. Heart rate was continuously recorded using a heart rate monitor (Polar H10).

    Time frame: Heart rate was continuously recorded during the test (every 1 s), until exhaustion. The highest heart rate at the time of exhaustion was recorded.

07

Study locations

1 site
  • Stefanos Karalis Indoors Facilities
    Athens, Byron 16231, Greece
08

References and documents

Publications

  • Pickering C, Grgic J. Caffeine and Exercise: What Next? Sports Med. 2019 Jul;49(7):1007-1030. doi: 10.1007/s40279-019-01101-0. PubMed 30977054 ↗
  • 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 ↗
  • Claudino JG, Gabbett TJ, Bourgeois F, Souza HS, Miranda RC, Mezencio B, Soncin R, Cardoso Filho CA, Bottaro M, Hernandez AJ, Amadio AC, Serrao JC. CrossFit Overview: Systematic Review and Meta-analysis. Sports Med Open. 2018 Feb 26;4(1):11. doi: 10.1186/s40798-018-0124-5. PubMed 29484512 ↗

Individual participant data

Plan to share: Yes — All IPD that underlie results in a publication

Supporting information: Study protocol, Sap, Icf

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 26, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06891469
Lead sponsor
Democritus University of Thrace
Responsible party
ZOI KONIDARI (DIETICIAN-NUTRITIONIST, Democritus University of Thrace) — Principal investigator
First posted
Mar 24, 2025
Start date
Jan 22, 2022
Primary completion
May 29, 2022
Completion
May 29, 2022
Last update
Mar 26, 2025

Study contacts

ILIAS SMILIOS, Professor
study director · Democritus University of Thrace
VASSILIS MOUGIOS, Professor
study director · Aristotle University Of Thessaloniki
GREGORY C. BOGDANIS, Professor
study chair · Gregory C. Bogdanis National and Kapodistrian University of Athens, School of Physical Education and Sport Science

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion