Effects of Creatine and Heat Exposure on Exercise Performance and Body Water Distribution

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18-27
SponsorUniversity of Windsor

About this trial

The goal of this clinical trial is to learn whether creatine supplementation changes how the body adapts to repeated exercise in the heat in healthy recreationally active adults and varsity athletes. The study will also examine whether creatine affects fluid balance, blood volume changes and exercise performance.

The main questions it aims to answer are:

Does creatine supplementation increase plasma volume and total body water during repeated heat exposure more than placebo? Does creatine supplementation improve exercise performance after heat acclimation more than placebo? Does creatine supplementation influence cardiovascular responses to heat stress?

Researchers will compare a creatine supplementation group to a placebo group to determine whether creatine changes the magnitude of heat acclimation adaptations.

Participants will:

Complete baseline measurements of body composition, hydration, blood markers, and exercise performance.

Consume either creatine monohydrate or a placebo supplement daily Complete repeated supervised exercise sessions in a controlled heated environment Undergo repeated assessments of body water, temperature, heart rate, and exercise performance throughout the study

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Healthy biological males between 18 and 27 years of age

Recreationally active males and varsity athletes

Able to safely participate in moderate-intensity exercise and heat exposure

Willing to maintain habitual diet and physical activity throughout the study

Disqualifiers

History of cardiovascular, metabolic, respiratory, renal, neurological, or heat-related illness

Contraindications to exercise testing or heat exposure identified during health screening

Current musculoskeletal injury limiting exercise participation

Current use of creatine supplementation or inability to complete the required washout period

Trial design

Design model

Parallel

Treatments tested in this trial

  • Creatine Monohydrate

    Dietary supplement

    Participants assigned to this intervention will consume micronized creatine monohydrate during a 7-day loading phase at 0.3 g·kg-¹·day-¹ followed by a maintenance dose of 0.03 g·kg-¹·day-¹ during the heat acclimation protocol. Supplements will be dissolved in orange juice and consumed under supervision during laboratory visits. Creatine supplementation will continue throughout the heat acclimation period.

  • Maltodextrin (Placebo)

    Dietary supplement

    Participants will consume maltodextrin matched to creatine supplementation appearance and dosing schedule during the loading and maintenance phases of the study.

Treatment groups

25 Participants
are divided into 2 treatment groups
Group A: Creatine Monohydrate + Heat ExposureExperimental treatment 1 intervention
Group B: Placebo + Heat ExposurePlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Plasma Volume Change Following Heat Acclimation and Creatine Supplementation

Percent change in plasma volume estimated from capillary blood hematocrit measurements. Following centrifugation, packed red blood cell volume and plasma layers will be measured using a microhematocrit reader, and hematocrit will be expressed as a percentage of total blood volume. Relative changes in blood volume and plasma volume will be inferred from repeated hematological measurements obtained at standardized time points throughout the study.

Time frame
Measured at baseline (pre-supplementation), after 7 days of creatine/placebo loading, and after 7 days of heat acclimation.

Secondary outcomes

1

Change in Total Body Water

Total body water measured using bioelectrical impedance analysis (InBody 230).

Time frame
Measured at baseline (pre-supplementation), after 7 days of creatine/placebo loading, and after 7 days of heat acclimation.
2

Change in Intracellular Water

Intracellular water estimated using bioelectrical impedance analysis.

Time frame
Measured at baseline (pre-supplementation), after 7 days of creatine/placebo loading, and after 7 days of heat acclimation.
3

Change in Extracellular Water

Extracellular water estimated using bioelectrical impedance analysis.

Time frame
Measured at baseline (pre-supplementation), after 7 days of creatine/placebo loading, and after 7 days of heat acclimation.
4

Change in VO₂ Peak

VO₂ peak assessed during supramaximal cycling exercise using breath-by-breath metabolic gas analysis.

Time frame
Measured at baseline (pre-supplementation), after 7 days of creatine/placebo loading, and after 7 days of heat acclimation.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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