Skip to content

The Effectiveness of Emergency Room Protocols for Treating Hyperthermia

The Effectiveness of Emergency Room Protocols for Treating Hyperthermia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07433036
Acronym
EDCP
Enrollment
50
Registered
2026-02-25
Start date
2025-07-01
Completion date
2028-12-31
Last updated
2026-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperthermia

Keywords

Hyperthermia, Exercise

Brief summary

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).

Interventions

During recovery, participants lie supine in an air-conditioned room

PROCEDURECooling packs

During recovery, participants lie supine while ice packs are applied to both sides of the neck, both arm pits, and both sides of the groin

PROCEDUREIce sheets

During recovery, participants are wrapped in bed sheets that have been soaked in ice water, while an electric fan blows air across their body

PROCEDUREBody bag cooling

During recovery, participants are placed in a body bag full of ice, and then have ice placed on top of their body, followed by zipping the body bag closed.

During recovery, participants are submerged in a bath, up to their neck, in cold water water with ice

Sponsors

University of Colorado, Colorado Springs
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Active, healthy individuals

Exclusion criteria

* Pregnant or planning on becoming pregnant * Have a pacemaker * Currently taking any prescribed or over the counter medications or nutritional supplements known to influence thermoregulatory responses * Experience lingering pain from a previous musculoskeletal injury (i.e. knee, hip, or back pain) * Use tobacco/nicotine products

Design outcomes

Primary

MeasureTime frameDescription
Rectal temperature cooling rateThe measurement occurs immediately upon completion of the exercise protocol. Time itself is part of the outcome variable and will vary between participants (~3 to 40 min post exercise protocol).Following termination of the exercise protocol, at a core temperature above 39 degrees Celcius, participants will be cooled until they reach a core temperature of 38 degrees Celcius. The cooling rate in degrees Celcius per minute, is the primary outcome.

Countries

United States

Contacts

CONTACTNathan Morris, PhD
nmorris6@uccs.edu719-255-4466

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026