Carbohydrate Mouth Rinsing and Softball Batting Performance

October 23, 2024 updated by: Chih-Hui Chiu, National Taiwan Sport University

Carbohydrate Mouth Rinsing and Softball Batting Performance: a Double-blind Crossover Study

Participants rinsed their mouths for 20 seconds with 25 ml of either 6.4% maltodextrin (CMR) or placebo (PLA). After rinsing, the grip force, counter-movement jump (CMJ) and batting tests were performed in sequence.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The purpose of this study was to investigate the effect of CMR on softball batting performance. Fourteen trained collegiate female softball players completed two trials in a randomization crossover trail, in which they rinsed their mouths for 20 seconds with 25 ml of either 6.4% maltodextrin (CMR) or placebo (PLA). After rinsing, the grip force, counter-movement jump (CMJ) and batting tests were performed in sequence. The tanner tee was utilised to perform five sets of five balls at a time, with a minimum of 3 minutes rest between sets. The batting test recorded average exit velocity, maximum exit velocity and batting accuracy. The standardized standard deviation (SD) for launch angle represents standardized variability.

Study Type

Interventional

Enrollment (Actual)

14

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • North
      • Taichung, North, Taiwan, 404
        • National Taiwan University of Sport

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • more than 6 years of professional fast-pitch softball training
  • more than 6 months of continuous training
  • from at least the top four teams in the country

Exclusion Criteria:

  • non-professionally fast-pitch softball training
  • lack of regular training in the past 6 months
  • in the event that the applicant has sustained a sports injury or is currently experiencing epilepsy, hypertension, hyperlipidemia, heart disease, arthritis, osteoporosis, or a brain injury, and has yet to undergo a period of recuperation exceeding three months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Carbohydrate mouth rinsing
Carbohydrate mouth rinsing for 20 seconds with 25 ml of 6.4% maltodextrin
The effects of placobo mouth rinsing on softball batting performance
Other Names:
  • plocabo mouth rinsing
Placebo Comparator: placebo
Mouth rinsing for 20 seconds with 25 ml of water
The effects of placobo mouth rinsing on softball batting performance
Other Names:
  • plocabo mouth rinsing

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
exit velocity
Time Frame: 20 seconds after rinsing
The average exit velocity
20 seconds after rinsing

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
batting accuracy
Time Frame: 20 seconds after rinsing
The standardized standard deviation (SD) for launch angle represents standardized variability
20 seconds after rinsing

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Chih Hui Chiu, PhD, National Taiwan University of Sport

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 30, 2022

Primary Completion (Actual)

May 30, 2022

Study Completion (Actual)

August 30, 2022

Study Registration Dates

First Submitted

October 22, 2024

First Submitted That Met QC Criteria

October 23, 2024

First Posted (Actual)

October 26, 2024

Study Record Updates

Last Update Posted (Actual)

October 26, 2024

Last Update Submitted That Met QC Criteria

October 23, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 113-8

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

no share plan

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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