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Skin Surface and Intradermal Temperature Responses to Heat Stress

Not Applicable
Recruiting
Conditions
Hyperthermia
Interventions
Other: Ambient Heating
Registration Number
NCT06593067
Lead Sponsor
University of Texas Southwestern Medical Center
Brief Summary

The purpose of this study is to compare surface and intradermal skin temperature responses to heat stress with and without evaporative and convective cooling.

Detailed Description

Humans have important thermoregulatory responses aimed at maintaining body temperature within a narrow range. These responses are driven in part by receptors located in the skin that monitor temperature changes and provide feedback to the central nervous system. Given that skin temperature can affect the physiological responses to heat stress, it is important to accurately measure skin temperature in response to heat stress with and without evaporative (i.e., sweat) and convective (i.e., air flow) cooling. Skin temperature is most often measured on the surface of the skin; however, this temperature can be influenced by other factors such as the local environment. It is unclear how the temperature of the skins surface compares to the temperature within the dermal layer of the skin.

The study team will directly compare skin surface and intradermal temperature responses to heat stress and determine whether these responses area altered by evaporative or convective cooling methods. To accomplish this objective, healthy adults will be exposed to ambient heat stress (no higher than 47°C) with and without evaporative (water sprayed on the skin) and convective (electric fan) cooling. Thermoregulatory responses, inclusive of skin surface and intradermal temperatures, will be assessed throughout the heat trial.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Free of any significant underlying medical problems based upon a detailed medical history and physical exam.
  • Normal resting electrocardiogram.
Exclusion Criteria
  • Known heart disease; other chronic medical conditions requiring regular medical therapy including cancer, diabetes, neurological diseases, and uncontrolled hypertension, etc.; as well as serious abnormalities detected on routine screening.
  • Individuals who are pregnant, planning to become pregnant, or breastfeeding.
  • Taking prescribed medications (such as beta blockers and non-dihydropyridine calcium channel blockers) or over-the-counter medications that have known influences on thermoregulatory response.
  • Current smokers, as well as individuals who regularly smoked within the past 3 years.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Healthy Adults ArmAmbient HeatingHealthy Subject will rest in an environmental chamber that is no hotter than 47°C (117 °F). While in the chamber, the study team will periodically use a water spray to wet subject's skin and turn on an electric fan. During this time, the temperature of skin on arm using a temperature probe placed on the surface of skin and another temperature probe placed within skin (intradermal) will be monitored.
Primary Outcome Measures
NameTimeMethod
Skin Temperature with Fan Only40 minutes into the heat intervention.

Skin temperature will be measured from small temperature sensitive electrodes attached to the surface and intradermal layer of the skin of the participant with the fan cooling modality.

Skin Temperature with Fan and Water Spray60 minutes into the heat intervention.

Skin temperature will be measured from small temperature sensitive electrodes attached to the surface and intradermal layer of the skin of the participant with both the fan and water spray cooling modalities.

Skin Temperature with Water Spray Only1 hour 20 minutes into the the heat intervention.

Skin temperature will be measured from small temperature sensitive electrodes attached to the surface and intradermal layer of the skin of the participant with the water spray cooling modality.

Skin Temperature with No Cooling20 minutes into the heat intervention.

Skin temperature will be measured from small temperature sensitive electrodes attached to the surface and intradermal layer of the skin of the participant during the heat intervention with no cooling.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Institute for Exercise and Environmental Medicine

🇺🇸

Dallas, Texas, United States

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