- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05302739
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
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.
Sponsor
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
Additional Relevant MeSH Terms
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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