MedPath

Cardiovascular Responses to Heat Waves in the Elderly

Active, not recruiting
Conditions
Hyperthermia
Aging
Interventions
Other: Simulated heat wave
Registration Number
NCT04538144
Lead Sponsor
University of Texas Southwestern Medical Center
Brief Summary

The purpose of this study is to assess the cardiovascular responses of the elderly to heat wave conditions

Detailed Description

Heat waves are lethal and cause a disproportionate number of deaths in the elderly relative to any other age group. It is important to note that such deaths are primarily cardiovascular, not hyperthermia itself, in origin. Nevertheless, we know relatively little about the effects of aging on cardiovascular function during actual heat wave-like conditions. The central hypothesis of this work is that the elderly exhibit greater cardiovascular stress during heat wave conditions. Aim 1 will test the hypothesis that recognized impairments in thermoregulatory capacity in the elderly will culminate in heightened cardiovascular stress during prolonged exposure to heat wave conditions. Comprehensive cardiovascular and thermal responses in the elderly, relative to younger adults, will be evaluated during exposure to two prolonged heat wave conditions: hot and humid (replicating the 1995 Chicago heat wave), very hot and dry (replicating the 2018 Los Angeles heat wave). The expected outcome from this body of work will re-shape our understanding of the consequences of aging on cardiovascular function during heat waves

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Healthy male and female individuals
  • 18-35 years or 65+ years of age
  • Free of any underlying moderate to serious medical conditions
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Exclusion Criteria
  • Known heart disease; other chronic medical conditions requiring regular medical therapy including cancer, diabetes, neurological diseases, uncontrolled hypertension, and uncontrolled hypercholesterolemia.
  • Taking of any medications (such as beta blockers and non-dihydropyridine calcium channel blockers) that have known influences on either cardiac function or sweating responses.
  • Abnormalities detected on routine screening.
  • Individuals who participate in a structured aerobic exercise training program at moderate to high intensities.
  • Current smokers, as well as individuals who regularly smoked within the past 3 years.
  • Body mass index of greater than 30 kg/m^2
  • Pregnant individuals
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Younger participantsSimulated heat waveIndividuals aged 18-39 years
Older participantsSimulated heat waveIndividuals aged 65 years or older
Primary Outcome Measures
NameTimeMethod
Core body temperaturePrior to and throughout each simulated heat wave exposure; an average of 480 minutes.

Core body temperature will be measured from gastrointestinal temperature via an ingestible telemetric pill.

Measures of left ventricular functionPrior to, during, and after each simulated heat wave exposure; approximately 20 min each

Measures of left ventricular function, such as ventricular wall motion and ventricular filling, will be obtained from echocardiography images.

Secondary Outcome Measures
NameTimeMethod
Arterial blood pressurePrior to and throughout each simulated heat wave exposure; an average of 480 minutes.

Arterial blood pressure will be measured using a standard arm blood pressure cuff

Cardiac outputPrior to, during, and after each simulated heat wave exposure; approximately 20 min each

Cardiac output (how much blood is ejected from the heart) will be measured using echocardiography and nitrous oxide rebreathing approaches.

Heart ratePrior to and throughout each simulated heat wave exposure; an average of 480 minutes.

Heart rate will be measured from ECG electrodes attached to the participant

Skin temperaturePrior to and throughout each simulated heat wave exposure; an average of 480 minutes.

Skin temperature will be measured from small temperature sensitive electrodes attached to the participant's skin

Cerebral perfusionPrior to, during, and after each simulated heat wave exposure; approximately 20 min each

Cerebral perfusion will be measured by doppler ultrasound of the internal carotid and vertebral arteries

Trial Locations

Locations (1)

Texas Health Presbyterian Hospital Dallas

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Dallas, Texas, United States

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