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Effect of Aging and Aerobic Fitness Level on Heat Dissipation

22 de enero de 2020 actualizado por: Petros Dinas

Effect of Aging and Aerobic Fitness Level on Heat Dissipation in Neutral Conditions

In the context of global aging, the health risk factors associated with exercising or working in the heat for aging population are exacerbated by the rising in global surface temperatures. The purpose of this investigation is to determine at what age the heat loss decrements occur and to examine if aerobic fitness level can affect the heat loss capacity in neutral environmental conditions.

Descripción general del estudio

Estado

Terminado

Intervención / Tratamiento

Descripción detallada

All trials were conducted to indoor gyms with the same environmental temperature and relative humidity, 26 - 30oC and 40-50% respectively, to ensure no difference in body temperature were due to the external thermal stress. The participants were instructed to refrain from intense exercise as well as alcohol and caffeine consumption for 24 hours prior to experimental trial and to had a light meal 2h before their arrival.

Upon arrival, participants would have to wear running shoes, light and short running shorts and light cotton socks. Participants received comprehensive instructions about the shuttle run test and the whole process of measurements. Firstly participants answered the International Physical Activity Questionnaire (IPAQ). Thereafter, anthropometrics data (weight and height) were evaluated as well as the body temperature in external ear canal and axillary. All participants followed five minutes warming up and then performed to 20 m shuttle run test until their volitional limit. Once the participants could no longer run, the test was over and the number of laps was recorded. After the end of the shuttle run, were evaluated the body temperature and the weight of each participants. No fluids consumptions were permitted until the second weighing. They were weighed twice, at baseline and at the end of the running test with a precision weight scale (Kern DE 150K2D, KERN & SOHN GmbH, Balingen, Germany).

Environmental data including air temperature and relative humidity were measured continuously using a portable weather station (LCD Digital Temperature & Humidity Meter HTC-1). The weather station was placed 1 meter above the ground according to the manufacturer's guidelines.

Tipo de estudio

Intervencionista

Inscripción (Actual)

431

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Thessaly
      • Trikala, Thessaly, Grecia, 42100
        • Department of Exercise Science, University of Thessaly
      • Tríkala, Thessaly, Grecia, 42100
        • FAME Lab, Department of Exercise Science, University of Thessaly

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

9 años a 60 años (Niño, Adulto)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Healthy children and adults

Exclusion Criteria:

  • Diagnosed chronic medical condition;
  • Symptoms of acute illness;
  • Recent (past 4 weeks) usage of medications known to affect the circulatory system, the thyroid, the pituitary function, or the metabolic status

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Shuttle run test
At the shuttle run test, participants were required to run between two lines 20 meters apart, while keeping pace with audio signals emitted from a pre-recorded CD. The frequency of the sound signals increases in such way that running speed was increased by 0.5 km h-1 each minute from the starting speed 8.5 km h-1.
At the shuttle run test, participants were required to run between two lines 20 meters apart, while keeping pace with audio signals emitted from a pre-recorded CD. The frequency of the sound signals increases in such way that running speed was increased by 0.5 km h-1 each minute from the starting speed 8.5 km h-1.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Aerobic fitness level
Periodo de tiempo: Through study completion (a shuttle run test), an average of 15 minutes
Aerobic fitness level was defined by peak oxygen uptake (VO2peak). VO2peak was determined by a 20m shuttle run test. The number of the last announced stage and the equivalent maximal speed from participants' performance were used for its VO2peak estimation
Through study completion (a shuttle run test), an average of 15 minutes
Change from baseline ear canal temperature
Periodo de tiempo: Change from baseline to the end of study completion (a shuttle run test), an average of 15 minutes
Ear canal temperature was recorded twice, at baseline and at the end of the shuttle run test (three times each at the left ear and recorded the mean value), using ear thermometer (IR100, MicrolifeSwitzerland)
Change from baseline to the end of study completion (a shuttle run test), an average of 15 minutes
Change from baseline axillary temperature
Periodo de tiempo: Change from baseline to the end of study completion (a shuttle run test), an average of 15 minutes
Axillary temperature was recorded twice, at baseline and at the end of the shuttle run test, using the electronic digital thermometer (EcoTemp, OMRON, Japan)
Change from baseline to the end of study completion (a shuttle run test), an average of 15 minutes
Physical activity levels
Periodo de tiempo: Once before the shuttle run test
Physical activity of the subject in a usual week was recorded via International Physical Activity Questionnaire. Scores include steps/day and METs/week, with no lower and upper limit
Once before the shuttle run test
Change from baseline body weight
Periodo de tiempo: Change from baseline to the end of study completion (a shuttle run test), an average of 15 minutes
Weight was recorded twice, at baseline and at the end of the shuttle run test, using a precision weight scale (Kern DE 150K2D, KERN & SOHN GmbH, Balingen, Germany
Change from baseline to the end of study completion (a shuttle run test), an average of 15 minutes
Change from baseline whole Body Sweat Rate
Periodo de tiempo: Change from baseline to the end of study completion (a shuttle run test), an average of 15 minutes
Whole Body Sweat Rate was determined by the difference of the pre-test and post-test weight of the participants
Change from baseline to the end of study completion (a shuttle run test), an average of 15 minutes
Air temperature
Periodo de tiempo: Up to 30 minutes, during a one complete shuttle run test
Air temperature was measured continuously using a portable weather station (LCD Digital Temperature & Humidity Meter HTC-1placed) 1 meter above the ground according to the manufacturer's guidelines
Up to 30 minutes, during a one complete shuttle run test
Relative humidity
Periodo de tiempo: Up to 30 minutes, during a one complete shuttle run test
Relative humidity was measured continuously using a portable weather station (LCD Digital Temperature & Humidity Meter HTC-1) placed 1 meter above the ground according to the manufacturer's guidelines
Up to 30 minutes, during a one complete shuttle run test

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de mayo de 2014

Finalización primaria (Actual)

30 de octubre de 2018

Finalización del estudio (Actual)

30 de octubre de 2018

Fechas de registro del estudio

Enviado por primera vez

16 de enero de 2020

Primero enviado que cumplió con los criterios de control de calidad

22 de enero de 2020

Publicado por primera vez (Actual)

27 de enero de 2020

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

27 de enero de 2020

Última actualización enviada que cumplió con los criterios de control de calidad

22 de enero de 2020

Última verificación

1 de enero de 2020

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • 10. Aging and heat loss

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Ensayos clínicos sobre Shuttle run test

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