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Caffeinated Chewing Gum on Special Forces Performance

Caffeinated Chewing Gum on Special Forces Performance: a Cross-over Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06638372
Enrollment
16
Registered
2024-10-15
Start date
2024-10-05
Completion date
2025-05-30
Last updated
2025-06-26

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

Conditions

Caffeine, Placebo

Keywords

exercise performance

Brief summary

The purpose of this project is to investigate the effects of caffeine chewing gum on the cognitive functions and special operations capabilities of special forces.

Detailed description

Using a randomisation crossover design, 20-40 active-duty special forces members who had undergone leave and special forces reserve training were divided into a caffeine trial (CAF) and a placebo trail (PL). After chewing caffeine-containing gum containing 5 mg/kg (CAF group) or caffeine-free gum (PL group) for 15 minutes, then performed a simple reaction test, a stroop test, a visual search test, a grip strength test, a vertical jump test, a 20-metre sprint test, and a counter-terrorism simulation test. A heart rate monitor was used to measure the heart rate and heart rate variability of the participants. Saliva samples were collected and analysed for α-Amylase, cortisol and caffeine concentrations before the test, after a 15-minute break from chewing gum and at the end of the test. Completion time of cognitive functions, grip strength, vertical jump height, 20 m sprint time, time to completion of the counterterrorism simulation test, and target score will be analysed using paired-sample t-tests.

Interventions

DIETARY_SUPPLEMENTcaffeine

The participants chewing either caffeine Gum (CAF trial, containing 3 mg/kg of caffeine) or Placebo Gum (PL) for 10 minutes. After rested for 15 minutes, the participants underwent tests.

Sponsors

National Taiwan Sport University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
MALE
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Active Special Warfare Unit members who have passed the Grade A Special Forces Reserve Training * No cardiovascular and joint diseases * Adult male over 20 years old

Exclusion criteria

* Non-active Special Warfare Unit members * Have cardiovascular and joint diseases * Under age

Design outcomes

Primary

MeasureTime frameDescription
Stroop task15 minutes after interventionThe color-word Stroop task were conducted using Psych/Lab for Windows. The reaction time (millisecond) were recorded.
visual search test15 minutes after interventionThe visual search test were conducted using Psych/Lab for Windows. The reaction time (millisecond) were recorded.

Secondary

MeasureTime frameDescription
anti-terrorist operations15 minutes after interventionTarget shooting and target finding. The completed time (seconds) were recorded.

Countries

Taiwan

Outcome results

None listed

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