The Repeatability of the Effect of Caffeine Supplementation on Submaximal Physiological Responses and Cycling Time Trial Performance

NCT ID: NCT06935214

Last Updated: 2025-04-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-05-01

Study Completion Date

2025-12-31

Brief Summary

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Recently, Grgic (2018) discussed the concept of responders and non-responders to caffeine supplementation highlighting the importance of the repeatability of results. However, the number of studies that have investigated this idea by repeating the same time-trial performance test multiple times with the same caffeine dose is sparse (Astorino et al., 2012; Del Coso et al., 2019). Furthermore, studies have shown that differences in the CYP1A2 genotype may account for some of the variation in time-trial performance (Guest et al., 2018). Thus, the current study aims to identify whether the effects of moderate caffeine supplementation (5 mg/kg) on time-trial performance are repeatable to aid the identification of responders and non-responders. Additionally, the study aims to determine if the CYP1A2 genotype may explain any of the variability in time-trial performance in trained male cyclists.

Detailed Description

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Conditions

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Caffeine

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Caffeine

5 mg/kg dose of caffeine (in pill form) - Trial 1

Group Type EXPERIMENTAL

Caffeine

Intervention Type DIETARY_SUPPLEMENT

5 mg/kg of caffeine in pill form

Caffeine

Intervention Type DIETARY_SUPPLEMENT

5 mg/kg dose of caffeine in pill form

Placebo

5 mg/kg dose of placebo (Maltodextrin in pill form) - Trial 2

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DIETARY_SUPPLEMENT

5 mg/kg dose of maltodextrin in pill form

Interventions

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Caffeine

5 mg/kg of caffeine in pill form

Intervention Type DIETARY_SUPPLEMENT

Placebo

5 mg/kg dose of maltodextrin in pill form

Intervention Type DIETARY_SUPPLEMENT

Caffeine

5 mg/kg dose of caffeine in pill form

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

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St. Mary's University, Twickenham

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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SMU_ETHICS_2024-25_992

Identifier Type: -

Identifier Source: org_study_id

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