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N/A N=41 Basic Science

Cardiovascular Responses to Heat Waves in the Elderly

Aging · Hyperthermia

Enrolled (actual)
41
Serious AEs
0.0%
Results posted
Aug 2025
Primary outcome: Primary: Change in Core Body Temperature — .68; 1.37; .58; 1.02 degrees Celsius (°C)

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Hot and Humid Trial (Other); Hot and Dry Trial (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Texas Southwestern Medical Center
Primary completion
Feb 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Core Body Temperature
.68; 1.37; .58; 1.02
PRIMARY
Change in Peak Mitral Annular Systolic Velocity (S')
1.46; 3.33; 1.39; 2.09
SECONDARY
Ending Skin Temperature
37.57; 37.37; 36.65; 36.05
SECONDARY
Ending Heart Rate
82; 87; 80; 81
SECONDARY
Ending Mean Arterial Pressure
77; 76; 78; 76
SECONDARY
Change in Cardiac Output
.88; .75; .38; .76

Summary

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

Eligibility Criteria

Inclusion Criteria

  • Healthy male and female individuals
  • 18-35 years or 65+ years of age
  • Free of any underlying moderate to serious medical conditions

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
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04538144). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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