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Load and Hold: Impact of 7-Day Creatine Monohydrate Loading on Breath-Hold Cycling Performance

Study acronym: BREATHE-C
StatusEnrolling by Invitation
PhaseNot applicable
Started
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Record status
This record was last updated November 18, 2025 (before its estimated November 26, 2025 completion). Its status may not reflect the trial's current state.

Record History

  1. Minor Study First Submitted
The present study aims to investigate the effects of creatine monohydrate supplementation on maximal breath-hold exercise performance on a bicycle ergometer in trained breath-hold divers. The testing protocol is specifically designed to replicate the physiological demands and exercise intensity of a maximal dynamic breath-hold dive. Creatine supplementation may improve breath-hold exercise capacity by acting as a rapid, anaerobic energy source that is independent of oxygen availability that does not generate fatigue-inducing metabolic byproducts. Furthermore, its intracellular buffering properties may help delay the onset of metabolic acidosis, thereby possibly prolonging muscular work under hypoxic conditions. Therefore, the main questions the study aims to answer are: 1. Can creatine monohydrate loading supplementation protocol improve breath-hold exercise performance by increasing total work (TW) and time to exhaustion (TTE)? 2. Can it will increase lactate threshold and delay the onset of the metabolic acidosis? Researchers will compare creatine monohydrate supplementation to a placebo (maltodextrin) to determine whether creatine improves maximal breath-hold exercise performance on a bicycle ergometer in trained breath-hold divers. Participants will: 1. Attend scheduled laboratory visits on 4 occasions (one for performing graded exercise test (GXT), one for familiarization with the breath-hold exercise (BHE) protocol, one for pre-supplementation BHE testing, one for post-supplementation BHE testing) 2. Take creatine monohydrate or a placebo for 7 days (5g four times per day) 3. Report any discomforts during supplementation period, log the type and frequency of their trainings 7 days prior to pre and post-supplementation testing, report everything they ate and drunk on the day prior to the pre and post-supplementation testing
Trial Details
NCT Number NCT07233707
Lead Sponsor Harokopio University
Collaborators: National and Kapodistrian University of Athens, University of Belgrade
Conditions
(from sponsor)
Healthy
Enrollment 26 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov