Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06907225

Physiological Responses to Heat Stress During High-risk Events

Led by United States Army Research Institute of Environmental Medicine · Updated on 2026-05-05

150

Participants Needed

2

Research Sites

65 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Exertional heat stroke (EHS) affects \~500 Military Personnel and over 100 Soldiers every year, and it is believed that these numbers are underreported. EHS is the most severe form of exertional heat illness (EHI) and can result in substantial, long-lasting organ damage, and even death in severe cases. Based on current knowledge and training needs, it is impossible to prevent every EHS - which shifts the focus from exclusively prevention to a combination of prevention, treatment, and enhancing recovery as much as possible. While many risk factors have been identified and there are adequate treatments available, biomarkers associated with heat stroke risk, recovery, and return-to-duty (RTD) remain largely unclear. The purpose of the proposed study is to enhance knowledge surrounding biomarkers of EHS and long-term health consequences that result from EHS. The investigators will recruit research volunteers for a field study in order to collect pre-, post-, and follow-up measures from a high-risk EHS event (i.e. ruck marches, timed runs) this will allow us to have a basis for comparison between Soldiers who collapse with EHS (from previously collected data) and those that complete high-risk events, but do not collapse. This will allow for comparison between the groups to identify EHS-specific biomarkers that could aid in recovery and RTD decisions for Soldiers.

CONDITIONS

Official Title

Physiological Responses to Heat Stress During High-risk Events

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals 18 years of age or greater, including cis- and transgender males and females and nonbinary
  • Current military service (active, Reserve, or National Guard)
  • Currently participating in training
Not Eligible

You will not qualify if you...

  • Females who are pregnant
  • Any individual currently on a physical profile that restricts running or foot marching
  • History of obstructive gastrointestinal diseases including diverticulosis, diverticulitis, inflammatory bowel disease, peptic ulcer disease, Crohn's disease, or ulcerative colitis
  • Scheduled MRI within 2 weeks after ingestion of core temperature pill
  • Known allergies to skin adhesive
  • Blood donation within the past 8 weeks

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 2 locations

1

Fort Novosel

Fort Novosel, Alabama, United States, 36362

Actively Recruiting

2

Field Study

Fort Jackson, South Carolina, United States, 29207

Not Yet Recruiting

Loading map...

Research Team

G

Gabrielle E Giersch, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here