Actively Recruiting
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
Eligibility Criteria
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
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
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
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
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