Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06907225

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

48 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Exertional heat stroke (EHS) is a serious condition affecting many military personnel each year, leading to potential long-lasting organ damage or death. Researchers are studying biomarkers that could help understand the risk, recovery, and safe return to duty after EHS. This observational study aims to compare soldiers who complete high-risk physical events without collapsing to those who experience EHS, to identify specific biomarkers related to heat stroke and its effects on heart, kidney, muscle, and liver function. Participants will be observed during events like ruck marches and timed runs, which are known high-risk activities for EHS. Data collection will include pre-event, post-event, and follow-up measurements such as core temperature, heart rate, and blood and urine biomarkers related to organ function. The study will monitor these markers up to 36 hours after exercise to assess physiological responses to heat stress and recovery patterns. During the study, participants will undergo various assessments including blood and urine tests every 6 hours for up to 36 hours, along with heart rate and core temperature monitoring during training. This will provide detailed information on the body's response to heat stress and help identify markers indicating successful recovery or risk. The study participation timeline includes training, immediate post-exercise monitoring, and follow-up to track changes over time.

CONDITIONS

Brief 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 (to include cis- and transgender males and females and nonbinary) 18 years of age or greater
  • 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 disease of the gastrointestinal tract including diverticulosis, diverticulitis, inflammatory bowel disease, peptic ulcer disease, Crohn's disease, ulcerative colitis
  • Scheduled MRI within 2 weeks after core temperature pill ingestion
  • Known allergies to skin adhesive
  • Blood donation in the past 8 weeks

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 36 hours after training

Participants who undergo routine military training are observed to collect physiological data related to heat stress during high-risk events.

Measurements collected during training and at least once every 6 hours for up to 36 hours after training

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

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Research Team

G

Gabrielle E Giersch, PhD

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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Published Research Related To This Trial

ACSM Expert Consensus Statement on Exertional Heat Illness: Recognition, Management, and Return to Activity.

William O Roberts, Lawrence E Armstrong, Michael N Sawka...

https://pubmed.ncbi.nlm.nih.gov/34524191