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Caffeinated Chewing Gum & Wrestling Performance

Not Applicable
Completed
Conditions
Caffeine
Control
Registration Number
NCT06758336
Lead Sponsor
National Taiwan Sport University
Brief Summary

The purpose of this study was to investigate the effect of caffeinated chewing gum on sympathetic nerve activity on wrestling simulation match.

Detailed Description

The purpose of this study was to investigated whether caffeine intake is effective in improving the performance of wrestlers in a simulated competition. The study was designed to involve 16 healthy adult male athletes who had been trained in professional wrestling and were divided into caffeine trial (CAF trial) and placebo trial (PL trial) in a randomized crossover double-blind study design. After three days of dietary control, participants arrived at the laboratory in the afternoon of the day of the trial to collect saliva samples in a quiet state and were fitted with a heart rate monitor. Participants chewed either caffeine-containing gum at 3 mg/kg body weight (CAF trial) or placebo-containing gum without caffeine (PL trial) for 10 minutes and then spit it out. Participants then underwent a 15-minute dynamic warm-up. At the end of the warm-up, participants performed 2 rounds of 3-minute wrestling-specific simulated matches, and the number of falls in the simulated matches was recorded. After the simulation match, saliva samples were collected from the participants again. The saliva samples were analyzed for caffeine alpha-amylase concentration. Differences between the two trials were analyzed using a paired sample t-test and significance was set at α\<0.05.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
16
Inclusion Criteria
  • more than 6years of professional wrestling training;
  • more than 6 months of continuous training;
  • recovering from sports injuries such as strains and contusions for at least 3 months.
Exclusion Criteria
  • non-professionally wrestling athlete;
  • none regular training in the past 6 months;
  • less than 3 months of recovery from a sports injury, or present epilepsy, hypertension, hyperlipidemia, heart disease, arthritis, osteoporosis, or brain injury;
  • a history of caffeine allergy.

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
The number of falls in the simulated matches15 minutes after intervention

Record number of falls in the simulated matches

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

National Taiwan University of Sport

🇨🇳

Taichung, North, Taiwan

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