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CompletedNCT06431035Updated Jul 24, 2024

Caffeine & Bodybuilding Dehydration Ability

An interventional study of caffeine in Caffeine and Placebo, sponsored by Chih-Hui Chiu. Completed at 1 site in Taiwan. Open to male participants aged 20 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-07-24.

Sponsored by Chih-Hui Chiu · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
14
Allocation
Randomized
Ages
20 Years to 40 Years
Sex
Male
01

Study summary

15-20 trained bodybuilding athletes were divided into caffeine gum trial (CAF) and placebo trial (PL) with a randomized, double-blind study design. The participants chewing either caffeine Gum (CAF trial, containing 5 mg/kg of caffeine) or placebo gum (PL) for 10 minutes. After rested for 15 minutes, Participants used the bicycle to adjust the pedal resistance and speed according to their own feelings until they were dehydrated to 2% of their original body weight.

Read the detailed description

The purpose of this study was to investigate the effect of caffeinated chewing gum on dehydration ability in bodybuilding athletes. Methods: 15-20 trained bodybuilding athletes were divided into caffeine gum trial (CAF) and placebo trial (PL) with a randomized, double-blind study design. The participants chewing either caffeine Gum (CAF trial, containing 5 mg/kg of caffeine) or placebo gum (PL) for 10 minutes. After rested for 15 minutes, Participants used the bicycle to adjust the pedal resistance and speed according to their own feelings until they were dehydrated to 2% of their original body weight. Record time from exercise to completion of dehydration, heart rate, HRV, energy expenditure, fat oxidation rate and carbohydrate oxidation rate.

02

Conditions studied

  • Caffeine
  • Placebo

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03

In context

Dehydration

204 studies on the registry are indexed under Dehydration; 29 are open to participants now.

This study's enrollment of 14 is below the median of 43 across 147 interventional studies indexed under Dehydration.

Browse Dehydration studies →

Lead sponsor

Chih-Hui Chiu is the lead sponsor of 6 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
20 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  • having won the top 8 places in a national competition,
  • having no cardiovascular or joint diseases
  • being an adult male

Exclusion criteria

Exclusion Criteria:

  • no top 8 finishes at national level
  • cardiovascular or joint disease, or any other condition that could be impaired by exercise
  • female and underage participants
  • previous caffeine allergy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Investigator)
Enrollment
14 participants (actual)

Study arms

  • Experimental
    caffeine gum

    Chewing caffeine Gum (CAF trial, containing 5 mg/kg of caffeine) for 10 minutes before test.

    Dietary Supplement: caffeine

  • Placebo comparator
    placebo

    Chewing placebo gum (without caffeine) for 10 minutes before test.

    Dietary Supplement: caffeine

Interventions

  • Dietary supplementcaffeine

    The participants chewed either caffeine gum (5 mg/kg for 10 minutes per chew) or a placebo (10 minutes per chew, using regular gum).

    Also known as: plocabo gum

06

What researchers measure

Primary outcomes

  1. dehydration speed

    The participants start dehydration until dehydrated to 2% of their original body weight.

    Time frame: 15 minutes after intervention

Secondary outcomes

  1. energy expenditure

    The energy expenditure during dehydration

    Time frame: 15 minutes after intervention

07

Study locations

1 site
  • National Taiwan University of Sport
    Taichung, 404, Taiwan
08

References and documents

Study documents

  • Study protocol · May 23, 2024

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No — Only participant number and experimental data are provided.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 24, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06431035
Lead sponsor
Chih-Hui Chiu
Responsible party
Chih-Hui Chiu (Professor, National Taiwan Sport University) — Sponsor-investigator
First posted
May 28, 2024
Start date
Apr 8, 2024
Primary completion
Jun 30, 2024
Completion
Jun 30, 2024
Last update
Jul 24, 2024

Study contacts

ChihHui Chiu, PhD
principal investigator · National Taiwan University of Sport

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 Jul 2024. You cannot join it, but the record below documents what was studied.

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