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Clinical Trials/NCT06308432
NCT06308432
Completed
Not Applicable

Sweat Rate Measurement With a Sensor (Wearable) in Different Climatic Conditions With Road Cyclists.

Universidad Católica San Antonio de Murcia1 site in 1 country12 target enrollmentFebruary 19, 2024
ConditionsSweat

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sweat
Sponsor
Universidad Católica San Antonio de Murcia
Enrollment
12
Locations
1
Primary Endpoint
Sweat
Status
Completed
Last Updated
last year

Overview

Brief Summary

Controlled, double-blind, crossover clinical trial with six parallel arms depending on the combination of temperature and humidity (22º and 40% humidity, 35º 40% humidity and 35º and 65% humidity), with two differents intensity, to investigate and validate the physiological use of a sensor in recreational road cyclists.

Detailed Description

Subjects who meet the inclusion criteria will be recruited to participate in the clinical trial and perform the exercise sessions. The cyclists in the study will have to make 7 visits to the laboratory. At the first visit, their aerobic performance will be evaluated by an incremental test to exhaustion with gas analysis. And in the next 6 visits they will have to perform a sustained intensity exercise with different environmental conditions according to the combination of temperature, humidity and intensity.

Registry
clinicaltrials.gov
Start Date
February 19, 2024
End Date
May 20, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
Male

Investigators

Sponsor
Universidad Católica San Antonio de Murcia
Responsible Party
Principal Investigator
Principal Investigator

Francisco Javier López Román

Principal Investigator

Universidad Católica San Antonio de Murcia

Eligibility Criteria

Inclusion Criteria

  • Male cyclists with more than two years of cycling experience.
  • Perform tests without fatigue.
  • Road bike training at least twice a week.

Exclusion Criteria

  • Participants with chronic illness.
  • Have a long-term injury that prevents you from training in the previous month.
  • Inability to understand informed consent.
  • Use of diuretics in the month prior to or during the measurement period.

Outcomes

Primary Outcomes

Sweat

Time Frame: Change of baseline rate of sweet rate in six occasions (the first day, day 7, day, 14, day 21, day 28, day 35)

The amount of sweat will be measured by a sensor placed on the back.

Secondary Outcomes

  • Fatigue(Change of fatigue in six occasions (the first day, day 7, day, 14, day 21, day 28, day 35))
  • Microcapillary Blood(Change of baseline rate of sweet rate in six occasions (the first day, day 7, day, 14, day 21, day 28, day 35))
  • Heart Rate(Changes of heart rate in six occasions (the first day, day 7, day, 14, day 21, day 28, day 35))
  • Temperature on the forehead(Changes in Temperature on the forehead in six occasions (the first day, day 7, day, 14, day 21, day 28, day 35))
  • Temperature in the ear(Changes in Temperature in the ear in six occasions (the first day, day 7, day, 14, day 21, day 28, day 35))
  • Karolinska drowsiness scale(It will be measured the day after in six occasions (the first day, day 7, day, 14, day 21, day 28, day 35))
  • Sleep efficiency(Changes in the sleep efficiency in six occasions (the first day, day 7, day, 14, day 21, day 28, day 35))

Study Sites (1)

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