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The Effects of Caffeine on Exercise Physiology and Time-trial Performance in a Hot Environment

The Effects of Caffeine Supplementation on Exercise Physiology and Time-trial Performance in a Hot Environment

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07129200
Enrollment
15
Registered
2025-08-19
Start date
2025-08-22
Completion date
2026-06-30
Last updated
2025-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caffeine, Thermoregulation

Keywords

caffeine, thermoregulation, time trial, exercise physiology

Brief summary

Maintaining a stable core temperature is vital for physiological function; yet, exercise in heat can be problematic, and there is risk of exertional heat-related illness (Flouris & Schlader, 2015; Leyk et al., 2019; Périard et al., 2021; Tyler et al., 2016; Veltmeijer et al., 2015). While aerobic fitness improves heat tolerance (Alhadad et al., 2019), strategies like acclimation and pre-cooling also mitigate heat stress (Casadio et al., 2016; Lorenzo et al., 2010; Ross et al., 2013; Siegel et al., 2010). Caffeine, an ergogenic aid (Del Corso et al., 2011; John et al., 2024), is known to enhance performance via adenosine antagonism and increased catecholamines in normothermic environments (Fredholm et al., 1999; Graham & Spriet, 1991). However, effects in heat are inconsistent (Ganio et al., 2009; Zhang et al., 2014), possibly due to caffeine reducing the ability to thermoregulate effectively. Therefore, the aim of this study is to investigate the effects of a moderate dose of caffeine (5 mg/kg) on thermoregulation during a 30-minute running time trial in 35°C heat.

Interventions

Hot environment of 35 degrees Celsius

OTHERThermoneutral environment

Thermoneutral environment of 18 degrees Celsius

Sponsors

St. Mary's University, Twickenham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy trained runners

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Blood lactate concentrationFrom baseline to completion, up to 31 daysChange from baseline in blood lactate concentration measured at rest and at five different exercise intensities (65, 70, 75, 80, and 85% percent of maximal oxygen uptake) on a treadmill.
Heart rateFrom baseline to completion, up to 31 daysChange from baseline in heart rate measured at rest and at five different exercise intensities (65, 70, 75, 80, and 85% percent of maximal oxygen uptake) on a treadmill.
Rating of perceived exertionFrom baseline to completion, up to 31 daysChange from baseline in rating of perceived exertion measured (using the 6-20 Borg scale) at five different exercise intensities (65, 70, 75, 80, and 85% percent of maximal oxygen uptake) on a treadmill.
Oxygen uptakeFrom baseline to completion, up to 31 daysChange from baseline in oxygen uptake measured at five different exercise intensities (65, 70, 75, 80, and 85% percent of maximal oxygen uptake) on a treadmill.
Time trial performanceFrom baseline to completion, up to 31 daysChange from baseline in distance covered during a 30 minute time trial on a treadmill.

Contacts

Primary ContactMark Glaister
mark.glaister@stmarys.ac.uk+447957616552

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026