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Effect of Aging and Aerobic Fitness Level on Heat Dissipation

22 de janeiro de 2020 atualizado 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.

Visão geral do estudo

Status

Concluído

Intervenção / Tratamento

Descrição detalhada

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 estudo

Intervencional

Inscrição (Real)

431

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

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

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

9 anos a 60 anos (Filho, Adulto)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Prevenção
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Aerobic fitness level
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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

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Patrocinador

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

1 de maio de 2014

Conclusão Primária (Real)

30 de outubro de 2018

Conclusão do estudo (Real)

30 de outubro de 2018

Datas de inscrição no estudo

Enviado pela primeira vez

16 de janeiro de 2020

Enviado pela primeira vez que atendeu aos critérios de CQ

22 de janeiro de 2020

Primeira postagem (Real)

27 de janeiro de 2020

Atualizações de registro de estudo

Última Atualização Postada (Real)

27 de janeiro de 2020

Última atualização enviada que atendeu aos critérios de controle de qualidade

22 de janeiro de 2020

Última verificação

1 de janeiro de 2020

Mais Informações

Termos relacionados a este estudo

Termos MeSH relevantes adicionais

Outros números de identificação do estudo

  • 10. Aging and heat loss

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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