Title: ICARUS - Psycho-physiological Profiling of Low and High Heat-resilient Individuals

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversity of Thessaly

About this trial

The escalating environmental heat-stress associated with global warming is a societal challenge with large and potential harmful consequences for humans. Excess morbidity and mortality during heat waves provides strong evidence for fatal outcomes. However, it is unclear why some people are particularly vulnerable and get sick from hyperthermia, while others adapt and tolerate exposure.

The Icarus project aims to provide a psycho-physiological framework for improved mitigation of the health threats associated with global warming. Combining expertise in integrative thermal physiology, pharmacology, photobiology, psychology and machine learning, we will collaborate on comprehensive cross-scientific studies using controlled lab-exposure combined with investigations in ecological settings including vulnerable and highly tolerant people across populations from northern to southern Europe.

Advanced algorithms will be developed to generate personalized alerts and advising based on behavioral patterns, psychological profiling, predicted vulnerability and willingness to adopt resilience-building strategies.

Global warming is projected to continue towards the end of the 21st century and constitutes an increasing threat to human health unless we as individuals and collectively become better in preventing acute effects, as well as devise sustainable strategies to limit further anthropogenic warming of the climate system. Acutely, improved guidance is important for both individual and public health, where Icarus aims at providing a highly improved basis for preventing heat-related disease, advising or nudging people towards pro-health behavior, including smarter use of technologies to mitigate heat stress, or adjusting medication to reduce adverse effects during heat events. In support of the sustainability agenda, our framework also forms a novel basis for developing advising algorithms relevant for optimization of climate change mitigation policy-making.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age 18-65 years (or your protocol-specific age range)

Healthy as determined by medical history screening questionnaire

Able to provide written informed consent

Able to complete heat exposure and light exercise protocol

Disqualifiers

History of cardiovascular, metabolic, neurological, or dermatological disease

History of heat-related illness (e.g., heat stroke)

Use of medications affecting thermoregulation or cardiovascular function

Smoking or substance abuse

Trial design

Design model

Single group

Treatments tested in this trial

  • Controlled Heat and Ultraviolet Radiation Exposure Protocol

    Other intervention

    Participants undergo a standardized 4-hour laboratory-based environmental exposure protocol consisting of passive heat exposure (40°C, 30% relative humidity), simulated solar ultraviolet radiation (up to 3 Standard Erythema Doses), light exercise-induced heat stress using a cycle ergometer, and recovery. Physiological, cardiovascular, thermoregulatory, biochemical, and psychological responses are assessed repeatedly throughout the protocol. The intervention is designed to quantify individual heat tolerance and combined heat-UV physiological strain under controlled conditions.

Treatment groups

80 Participants
are divided into 1 treatment group
Group A: Standardized Heat and UV Exposure ProtocolExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Physiological Heat Tolerance

Maximum tolerable exposure time during the standardized heat and ultraviolet radiation protocol. (units of measure: Minutes)

Time frame
During 4-hour laboratory protocol
2

Heart Rate Response

Heart rate measured continuously during heat and UV exposure to assess cardiovascular strain \[unit: beats per minute (bpm)\]

Time frame
During 4-hour laboratory protocol

Secondary outcomes

1

Blood Pressure Response

Stroke volume assessed to evaluate cardiac function during environmental stress (unit: mL/beat)

Time frame
During 4-hour laboratory protocol
2

Cardiac Output

Ability to maintain blood pressure and consciousness during postural change following exposure (unit : L/min)

Time frame
During 4-hour laboratory protocol
3

Orthostatic Tolerance

Ability to maintain blood pressure and consciousness during postural change following exposure \[unit: time to presyncope (minutes)\]

Time frame
Every 60 min during the protocol
4

Echocardiographic Parameters

Cardiac structure and function assessed via echocardiography (ejection fraction) (unit:%)

Time frame
Every 60 min during the protocol

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Thessaly

Lead sponsor

University of Copenhagen

Collaborator

Bispebjerg Hospital

Collaborator