Efficacy of an Investigational Thermal Rehab Machine on Body Cooling in Hyperthermic Individuals
1 other identifier
interventional
14
1 country
1
Brief Summary
Exertional heat stroke (EHS) is an emergency medical condition that is prevalent in military soldiers, athletes, and laborers. It is diagnosed when the rectal temperature is above 40°C with the presence of central nervous dysfunction (altered mental status). The gold standard method of care for EHS is immediate onsite whole body cooling using cold-water immersion (cooling rates \>0.15°C•min-1), which is reported to have the highest cooling rate. In the treatment of EHS, selecting a cooling modality with a high cooling rate becomes crucial to minimize the time above the critical threshold of body temperature at 40°C to less than 30 minutes for the best chance of survival and to minimize the severity of prognosis. However, in situations where cold water immersion is not feasible (in certain military, firefighter, or other remote settings), other cooling modalities must be available that have a cooling capacity similar to that of cold-water immersion. In this proposed study, the investigators aim to examine the cooling rates of the Polar Breeze® device (developed by Statim Technologies, LLC, Clearwater, FL) compared to rotating ice towels, a cooling method often recommended by sports medicine professionals as an alternative to cold-water immersion, and passive rest in participants with exercise-induced hyperthermia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2018
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 15, 2018
CompletedFirst Posted
Study publicly available on registry
August 23, 2018
CompletedStudy Start
First participant enrolled
September 17, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2018
CompletedApril 18, 2019
April 1, 2019
4 months
August 15, 2018
April 16, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
Change in Internal Body Temperature
The rate at which body temperature is reduced during whole body cooling following exercise-induced hyperthermia.
0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60 minutes post onset of cooling
Study Arms (3)
Thermal rehab machine
EXPERIMENTALParticipants, following exercise-induced hyperthermia, will be cooled using a Thermal Rehab Machine (Polar Breeze, Statim Technologies, LLC, Clearwater Florida), which is a micro-environmental air chiller. The device will be placed over the subjects head and through trans pulmonary cooling, will cool the body.
Forearm Ice Towels
ACTIVE COMPARATORParticipants, following exercise-induced hyperthermia, will be cooled using forearm ice towels. Cotton-blend towels will be doused in ice-water and then wrapped around participant's forearms (elbow to wrist). The towels will be rotated (re-wetted) every 2 minutes)
Passive Cooling
NO INTERVENTIONParticipants, following exercise-induced hyperthermia, will undergo a period of passive rest to allow the body to cool via natural mechanisms of evaporation of sweat from the skin's surface and convection
Interventions
The Polar Breeze unit is a microenvironmental air-chiller. That means it is a single-pass air-conditioner capable of cooling external air
Towels that are wetted with ice water and wrapped around participants forearms (length of arm from wrist to elbow)
Eligibility Criteria
You may qualify if:
- male between the ages of 18-35.
- recreationally active (regularly exercise at a minimum of 4-5 times per week for greater than 30 minutes per session)
You may not qualify if:
- chronic health problems,
- fever or current illness at the time of testing
- history of cardiovascular, metabolic, or respiratory disease
- current musculoskeletal injury that limits physical activity
- history of exertional heat illness in the past three years.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of North Carolina, Greensborolead
- Statim Technologies, LLCcollaborator
Study Sites (1)
University of North Carolina at Greensboro
Greensboro, North Carolina, 27412, United States
Study Officials
- PRINCIPAL INVESTIGATOR
William M Adams, PhD
University of North Carolina, Greensboro
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- DEVICE FEASIBILITY
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
August 15, 2018
First Posted
August 23, 2018
Study Start
September 17, 2018
Primary Completion
December 31, 2018
Study Completion
December 31, 2018
Last Updated
April 18, 2019
Record last verified: 2019-04
Data Sharing
- IPD Sharing
- Will not share