The Effects of Facial Cooling on Fencing Performance

March 29, 2022 updated by: St Mary's University College

The Effects of Facial Cooling on Physiological and Perceptual Responses During Simulated Competition in Male Epee Fencers

Fencing competitions can last between nine and eleven hours, during which athletes wear layers of protective equipment that impair evaporative heat transfer and spend a large amount of time at exercise intensities > 85% maximum heart rate. Fencing performance can potentially contribute to heat stress due to increases in core temperature. Elevated core temperatures could hamper performance, and therefore the implementation of a strategy to reduce core temperature increases could lead to augmented fencing performance. Cooling methods are limited for use between fencing matches and during short breaks within a direct elimination match. Furthermore, due to multiple layers of thick protective equipment cooling method applications are limited primarily to the facial area. A potential cooling strategy, during fencing competition, includes the utilization of a water facial mist spray combined with fanning of the face. Therefore, the aim of this study is to investigate the novel use of facial cooling on core temperature, relevant physiological parameters, perceived exertion and thermal comfort and sensation during a simulated fencing competition performance, in male epee fencers.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

10

Phase

  • Not Applicable

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

18 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Trained fencers

Exclusion Criteria:

  • Injured or a contraindicative medical condition

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Facial cooling
Between each simulated fencing match participants will spend the first 30 s of rest having a facial water mist sprayed onto the face with accompanying fanning from 50 cm away from the face.
30 s of water mist sprayed onto the face during breaks in a simulated fencing competition
No Intervention: Placebo

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Tympanic temperature
Time Frame: From baseline to completion, up to 31 days
Change from baseline in tympanic temperature taken during each 60 s break within the simulated fencing bout protocol and between each simulated fencing bout
From baseline to completion, up to 31 days
Heart rate
Time Frame: From baseline to completion, up to 31 days
Change from baseline in heart rate recorded during each 60 s break within the simulated fencing bout protocol and between each simulated fencing bout
From baseline to completion, up to 31 days
Blood lactate concentration
Time Frame: From baseline to completion, up to 31 days
Change from baseline in blood lactate concentration recorded during each 60 s break within the simulated fencing bout protocol and between each simulated fencing bout
From baseline to completion, up to 31 days
Thermal comfort
Time Frame: From baseline to completion, up to 31 days
Change from baseline in thermal comfort will be recorded on a scale of 1 - 4 (1 = comfortable; 2 = slightly uncomfortable; 3 = uncomfortable; 4 = very uncomfortable) during each 60 s break within the simulated fencing bout protocol and between each simulated fencing bout.
From baseline to completion, up to 31 days
Thermal sensation
Time Frame: From baseline to completion, up to 31 days
Change from baseline in thermal sensation will be recorded on a scale of 1 - 7 (1 = cold; 2 = cool; 3 = slightly cool; 4 = neutral; 5 = slightly warm; 6 = warm; 7 = hot) during each 60 s break within the simulated fencing bout protocol and between each simulated fencing bout.
From baseline to completion, up to 31 days
Rating of perceived exertion of the dominant arm
Time Frame: From baseline to completion, up to 31 days
Change from baseline in rating of perceived exertion exertion for the dominant arm will be recorded on a scale of 1 - 10 (CR10 Borg Scale) during each 60 s break within the simulated fencing bout protocol and between each simulated fencing bout.
From baseline to completion, up to 31 days
Rating of perceived exertion of the legs
Time Frame: From baseline to completion, up to 31 days
Change from baseline in rating of perceived exertion for the legs will be recorded on a scale of 1 - 10 (CR10 Borg Scale) during each 60 s break within the simulated fencing bout protocol and between each simulated fencing bout.
From baseline to completion, up to 31 days
Rating of whole body perceived exertion
Time Frame: From baseline to completion, up to 31 days
Change from baseline in whole body rating of perceived exertion will be recorded on a scale of 1 - 10 (CR10 Borg Scale) during each 60 s break within the simulated fencing bout protocol and between each simulated fencing bout.
From baseline to completion, up to 31 days

Collaborators and Investigators

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

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 (Anticipated)

April 20, 2022

Primary Completion (Anticipated)

August 31, 2022

Study Completion (Anticipated)

September 26, 2022

Study Registration Dates

First Submitted

March 4, 2022

First Submitted That Met QC Criteria

March 29, 2022

First Posted (Actual)

March 31, 2022

Study Record Updates

Last Update Posted (Actual)

March 31, 2022

Last Update Submitted That Met QC Criteria

March 29, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • StMarysUC3

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

product manufactured in and exported from the U.S.

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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