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Caffeinated Gum Softball Performance

C

Chih-Hui Chiu

Status

Completed

Conditions

Caffeine

Treatments

Other: CAFFEINE GUM

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study was to investigate the effects of caffeinated chewing gum on female softball pitching and hitting performance. 24 trained female softball players (10 pitchers and 14 fielders) were divided into a caffeine chewing gum trial (CAF) or a placebo trial (PLA) in a single-blind, randomized, crossover experimental design. Two pieces of gum containing 100 mg of caffeine (CAF) or without caffeine (PLA) were chewed for 10 minutes and then spit out, followed by a 15-minute warm-up. The physical tests included grip strength and countermovement jump. The softball-specific tests included pitching (fast ball speed) or hitting (exit speed). The two trials were separated by seven days.

Full description

This study utilized a randomized, crossover, single-blind experimental design. At least two familiarization tests were conducted one week before the formal trial to ensure each participant was familiar with the experimental procedures. Before the first formal trial, participants were randomly assigned to either the caffeinated chewing gum trial (CAF) with 200 mg of caffeine or the placebo trial (PLA) without caffeine, seven days apart (Figure 1). The primary outcome was the pitching and hitting performance, and the secondary outcomes were hand grip strength and height of countermovement jump.

Enrollment

24 patients

Sex

Female

Ages

20 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

    1. adult female; 2. at least six years of professional softball training and familiarity with all softball skills; 3. caffeine intake of less than 80 mg daily.

Exclusion criteria

    1. not professionally trained; 2. having a medical condition for which exercise is not recommended, such as hypertension, hyperlipidemia, or heart disease; 3. having any musculoskeletal injuries within the last six months or not being able to complete a full trial; 4. having a history of caffeine allergy.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

24 participants in 2 patient groups, including a placebo group

caffeine gum
Experimental group
Description:
The gum containing 200 mg of caffeine (CAF) were chewed for 10 minutes before test
Treatment:
Other: CAFFEINE GUM
placebo
Placebo Comparator group
Description:
The gum without caffeine (PLA) were chewed for 10 minutes before test
Treatment:
Other: CAFFEINE GUM

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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