Skip to main content
OpenTrials
Completed

NCT Number: NCT03832504

Identifying Strategies to Alleviate Cardiovascular Stress in Coronary Patients During Heatwaves

The purpose of this study is to determine the optimal cooling strategies to alleviate cardiovascular strain of coronary artery disease individuals during a simulated North American and Australian heatwave.

Completed

Looking for future studies?

Notify Me

Key information

Age range

50 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

cardiovascular Prevention and rehabilitation Centre of the Montreal Heart Institute

Montreal, Quebec, H1T1N6, Canada

About this study

Globally, heatwaves are occurring more frequently, are of greater intensity and longer in duration. The devastating health impacts of extreme heat are increasingly recognized, particularly in vulnerable populations, such as adults with coronary artery disease (CAD). While the most effective cooling strategy during a heatwave is the use of air conditioning (AC), economical concerns can limit AC use among vulnerable populations. In addition, widespread AC use places a significant burden on the electrical grid, causing brown-outs and black-outs during periods of extreme heat.

Electric fans offer a cooling strategy with a 50-fold lower power requirement and cost compared to AC. However, the efficacy of fan use during heat waves remains contentious. The primary objective of this study is to identify the optimal cooling strategy to alleviate cardiovascular strain of CAD patients exposed to typical North American heatwave conditions (38°C with 60% relative humidity). The secondary objective is to identify the optimal cooling strategy to alleviate cardiovascular strain of CAD patients exposed to typical Australian heatwave conditions (46°C with 10% relative humidity).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • History of angiographic coronary disease (≥70% arterial diameter narrowing of at least one major epicardial coronary artery) and/or prior coronary revascularization and/or documented prior acute coronary syndrome and/or stable angina and/or perfusion defect during exercise testing.
  • No CAD-related hospitalisations or changes in cardiac medications or change in pattern of angina for at least 3 months prior to enrolment

Exclusion criteria

  • Body mass index ≥35 kg/m2.
  • Currently undertaking estrogen therapy.
  • Evidence of current fluid and electrolyte disorders, anemia, abnormal thyroid function, arrhythmias, diabetes, renal disease, liver disease, cerebrovascular disease, significant pulmonary disease, endocrine abnormalities, significant cognitive impairment, psychiatric disorder, substance abuse, degenerative neurological condition or any other medical condition deemed to pose risk during the proposed experiments.
  • Uncontrolled hypertension (>180/110 mmHg).
  • Recent (<3 months) coronary bypass surgery.
  • Ejection fraction <40% and/or clinical evidence/history of heart failure.
  • Significant valvular heart disease
  • Resting ECG abnormalities interfering with observation of ST segment changes during testing.

Treatment and study plan

No intervention

Other

The participant will rest in a seated position.

Fan

Other

A fan placed in front of the participant will provide an airflow of 4 m/s throughout the exposure.

Skin Wetting

Other

Tap water (~18°C) will be applied every 5 minutes to the face, neck, upper and lower arms and upper and lower legs using a spray bottle.

Fan + Skin wetting

Other

A fan placed in front of the participant will provide an airflow of 4 m/s throughout the exposure. In addition, tap water (~18°C) will be applied every 5 minutes to the face, neck, upper and lower arms and upper and lower legs using a spray bottle.

Primary outcomes

  1. Rate pressure product

    Time frame: Change from baseline to the end of the 3 hour exposure

    Rate pressure product, in beats per minute per mmHg

Secondary outcomes

  1. Body core temperature

    Time frame: Change from baseline to the end of the 3 hour exposure

    In degrees Celcius

Other outcomes

  1. Skin temperature

    Time frame: Change from baseline to the end of the 3 hour exposure

    In degrees Celcius

  2. Sweat loss

    Time frame: Change from baseline to the end of the 3 hour exposure

    In kilograms

  3. Local sweat rate

    Time frame: Measured continously during the 3 hour exposure

    In mg per minute per cm2

  4. Skin blood flow

    Time frame: Measured continously during the 3 hour exposure.

    In arbitrary perfusion units

Sponsors and collaborators

Lead sponsor

Montreal Heart Institute

Other

Collaborators

  • National Health and Medical Research Council, Australia

Registry information

Official study title

Identifying Optimal Cooling Strategies for Coronary Artery Disease Patients During Heatwaves

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Feb 6, 2019
Registry last updated
Aug 1, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.