Intermittent Cooling During Baseball Games on Hitting and Defense Performance

September 24, 2021 updated by: Chen Kang, National Taiwan Sport University

Intermittent Cooling During Baseball Games Alleviated Perceived Exertion But Had no Effect on Hitting and Defense Performance in Hot Environment

This study adopted a practical approach in intermittent cooling on forehead and neck during an intra-squad baseball game. Exit velocity of batted balls was used as an indicator for hitting performance and a baseball-specific reactive agility test to evaluate the cognitive performance in defense.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study used a randomized cross-over design. Each participant completed a cooling and a non-cooling trial in a random order, separated by a 20-day washout period. Each trial contained a 7-inning intra-squad game in hot environment. Hitting, reactive agility, and cognitive tests were administered before and after the game. Forehead skin and tympanic temperature, perceived exertion, and thermal sensation were measured during the game.

Experimental procedure After body weight and rectal temperature were measured in a temperature-controlled room, the participants consumed a standardized breakfast. The breakfast included white bread 1.2 g/kg, jam 0.1 g/kg, butter 0.l g/kg, and soybean milk 5 ml/kg (6.2 kcal/kg, containing carbohydrate 1.0 g/kg, protein 0.24 g/kg, and fat 0.14 g/kg). Go/NoGo and Stroop Color-Word tasks were administered after breakfast. After finishing the cognitive tests, the participants moved to the field for self-selected warm up, followed by hitting and reactive agility tests. After the intra-squad game, the participants repeated the hitting, reactive agility, and cognitive tests. The participants can drink water ad libitum during the experimental period.

Intra-squad game The 7-inning intra-squad games were played under the standard rules of baseball in hot environmental conditions (temperature 31.1-33.4℃, humidity 63-67%).

Cooling intervention The participants in the cooling trial put cold towels on their forehead and neck for 3 min in the shaded dugout during their offensive half innings when they were not scheduled to hit or on base. Each participant received the cooling intervention 3 to 4 times in each game. After each use, the towels were kept in a cooler that contained water mixed with ice and salt to keep the temperature at approximately 0℃. The participants in the control trial sat in the shaded dugout without any cooling intervention.

Measurement of temperature Rectal temperature was measured before breakfast and after the game with a digital thermometer fitted with disposable sheaths. Forehead skin and tympanic temperature were measured with infrared thermometers during their offensive half innings in the dugout.

Hitting test The participants used their own bat to hit balls thrown by a pitching machine positioned 12 m from the home plate. The ball speed was approximately 120 km/h. The participants were asked to make the best effort to hit the balls. Each test was consisted of 15 batted balls. Exit velocity was measured with a video system and swing power was measured with a sensor attached to the knob of the bat.

Reactive agility test The infielders played defense against ground balls at the short stop position while the outfielders played defense against fly balls in center field. The participants were asked to move toward the ball as soon as they determine the trajectory and make the best effort to catch it. Each test was consisted of 15 batted balls. The reaction time, the time from bat-ball contact to the participant's first definitive movement in the intended direction, was calculated post-hoc using frame-by-frame analysis of the video footage by an experienced coach

Cognitive tests The Go/NoGo and Stroop Color-Word tasks were administered on a laptop computer in a quiet room. Each task contained 100 trials.

Perceived exertion and thermal sensation The participants reported their perceived exertion and thermal sensation during their offensive half innings. Perceived exertion was estimated with a 10-point Borg scale. Thermal sensation was estimated with a 7-point scale from -3 being the coolest to 3 being the hottest.

Study Type

Interventional

Enrollment (Actual)

10

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

      • Taichung, 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

20 years to 23 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • baseball players from National Taiwan University of Sport, Taiwan
  • at least 6 years of experience in baseball training
  • have competed nationally.

Exclusion Criteria:

  • having cardiovascular or other known chronic diseases
  • taking any medication in the preceding 2 months
  • having musculoskeletal injuries in the preceding 2 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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: cooling
The participants in the cooling trial put cold towels on their forehead and neck for 3 min in the shaded dugout during their offensive half innings when they were not scheduled to hit or on base. Each participant received the cooling intervention 3 to 4 times in each game. After each use, the towels were kept in a cooler that contained water mixed with ice and salt to keep the temperature at approximately 0℃.
The participants in the cooling trial put cold towels on their forehead and neck for 3 min in the shaded dugout during their offensive half innings when they were not scheduled to hit or on base. Each participant received the cooling intervention 3 to 4 times in each game. After each use, the towels were kept in a cooler that contained water mixed with ice and salt to keep the temperature at approximately 0℃.
Placebo Comparator: Control
The participants in the control trial sat in the shaded dugout without any cooling intervention.
The participants in the control trial sat in the shaded dugout without any cooling intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
rectal temperature
Time Frame: baseline
baseline
change in rectal temperature
Time Frame: 5 hours after the baseline
5 hours after the baseline
forehead skin temperature
Time Frame: baseline
baseline
change in forehead skin temperature
Time Frame: 2 hours after the baseline
measured after each inning in an 2-hour 7-inning intra-squad baseball game
2 hours after the baseline
tympanic temperature
Time Frame: baseline
baseline
change in tympanic temperature
Time Frame: 2 hours after the baseline
measured after each inning in an 2-hour 7-inning intra-squad baseball game
2 hours after the baseline
exit velocity of batted balls
Time Frame: baseline
baseline
change in exit velocity of batted balls
Time Frame: 3 hours after baseline
3 hours after baseline
reactive agility in defense
Time Frame: baseline
The reaction time, the time from bat-ball contact to the participant's first definitive movement in the intended direction
baseline
change in reactive agility in defense
Time Frame: 3 hours after baseline
The reaction time, the time from bat-ball contact to the participant's first definitive movement in the intended direction
3 hours after baseline
swing power
Time Frame: baseline
power of bat swings
baseline
change in swing power
Time Frame: 3 hours after baseline
power of bat swings
3 hours after baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ratings of perceived exertion
Time Frame: baseline
baseline
change in ratings of perceived exertion
Time Frame: 2 hours after baseline
measured after each inning in an 2-hour 7-inning intra-squad baseball game
2 hours after baseline
thermal sensation
Time Frame: baseline
baseline
change in thermal sensation
Time Frame: 2 hours after baseline
measured after each inning in an 2-hour 7-inning intra-squad baseball game
2 hours after baseline
Go/NoGo tasks
Time Frame: baseline
reaction time and error rate
baseline
change in Go/NoGo tasks
Time Frame: 5 hours after baseline
reaction time and error rate
5 hours after baseline
Stroop Color-Word test
Time Frame: baseline
reaction time and error rate
baseline
change in Stroop Color-Word test
Time Frame: 5 hours after baseline
reaction time and error rate
5 hours after baseline

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Chen-Kang Chang, 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)

July 15, 2020

Primary Completion (Actual)

September 10, 2020

Study Completion (Actual)

September 10, 2020

Study Registration Dates

First Submitted

September 6, 2021

First Submitted That Met QC Criteria

September 24, 2021

First Posted (Actual)

October 6, 2021

Study Record Updates

Last Update Posted (Actual)

October 6, 2021

Last Update Submitted That Met QC Criteria

September 24, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 18-076-A

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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