- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06659185
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
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:
|
|
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:
|
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.
Sponsor
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
Keywords
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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