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

U

Universidad Católica San Antonio de Murcia

Status

Completed

Conditions

Sweat

Treatments

Other: Low temperature
Other: Low intensity
Other: High temperature
Other: High humidity
Other: High intensity
Other: Low Humidity

Study type

Interventional

Funder types

Other

Identifiers

NCT06308432
UCAMCFE-00036

Details and patient eligibility

About

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.

Full 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.

Enrollment

12 patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

12 participants in 6 patient groups

22 degrees, 40% humidity and 50% intensity
Experimental group
Description:
The room in which the 30-minute test will be performed will be at 22 degrees Celsius and 40% humidity. The subject should perform the test at 50% of the power at which he reached his VO2max.
Treatment:
Other: Low Humidity
Other: Low intensity
Other: Low temperature
35 degrees, 40% humidity and 50% intensity
Experimental group
Description:
The room in which the 30-minute test will be performed will be at 35 degrees Celsius and 40% humidity. The subject should perform the test at 50% of the power at which he reached his VO2max.
Treatment:
Other: Low Humidity
Other: High temperature
Other: Low intensity
35 degrees, 65% humidity and 50% intensity
Experimental group
Description:
The room in which the 30-minute test will be performed will be at 35 degrees Celsius and 65% humidity. The subject should perform the test at 50% of the power at which he reached his VO2max.
Treatment:
Other: High humidity
Other: High temperature
Other: Low intensity
22 degrees, 40% humidity and 60% intensity
Experimental group
Description:
The room in which the 30-minute test will be performed will be at 22 degrees Celsius and 40% humidity. The subject should perform the test at 60% of the power at which he reached his VO2max.
Treatment:
Other: Low Humidity
Other: High intensity
Other: Low temperature
35 degrees, 40% humidity and 60% intensity
Experimental group
Description:
The room in which the 30-minute test will be performed will be at 35 degrees Celsius and 40% humidity. The subject should perform the test at 60% of the power at which he reached his VO2max.
Treatment:
Other: Low Humidity
Other: High intensity
Other: High temperature
35 degrees, 65% humidity and 60% intensity
Experimental group
Description:
The room in which the 30-minute test will be performed will be at 35 degrees Celsius and 65% humidity. The subject should perform the test at 60% of the power at which he reached his VO2max.
Treatment:
Other: High intensity
Other: High humidity
Other: High temperature

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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