Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT07433036

The Effectiveness of Emergency Room Protocols for Treating Hyperthermia

Led by University of Colorado, Colorado Springs · Updated on 2026-02-25

50

Participants Needed

1

Research Sites

182 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will help us as scientists and clinicians understand how effective commonly used cooling protocols in emergency departments are and which of the protocols is the most effective. It consists of a single, approximately 1 hour preliminary session and five, approximately 3 hour experimental sessions, equaling an approximate 16 hour total time commitment. The purpose of this research is to test the effectiveness of three cooling protocols. 1. Cooling packs 2. "Ice Sheets", which are bed sheets soaked in ice water, wrapped around the participant, while a fan blows air on them. 3. Body bag filled with ice, commonly used in emergency departments to treat hyperthermia Additionally, a negative control (passive cooling in air-conditioned room) and a positive control (cold water immersion).

CONDITIONS

Official Title

The Effectiveness of Emergency Room Protocols for Treating Hyperthermia

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Active, healthy individuals
  • Age between 18 and 65 years
Not Eligible

You will not qualify if you...

  • Pregnant or planning to become pregnant
  • Have a pacemaker
  • Taking prescribed or over-the-counter medications or nutritional supplements affecting thermoregulation
  • Experience lingering pain from a previous musculoskeletal injury such as knee, hip, or back pain
  • Use tobacco or nicotine products

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Colorado Colorado Springs

Colorado Springs, Colorado, United States, 80918

Actively Recruiting

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Research Team

N

Nathan Morris, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

5

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