Tarp Assisted Cooling of Hyperthermic Individuals
Primary Purpose
Healthy
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tarp Assisted Cooling
passive cooling
Sponsored by
About this trial
This is an interventional treatment trial for Healthy focused on measuring Heat, Cooling
Eligibility Criteria
Inclusion Criteria:
- Healthy
- Aerobic exercise at least twice weekly
Exclusion Criteria:
- History of exertional heat illness
Sites / Locations
- Center for Research and Exercise in Special Environments
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Sham Comparator
Arm Label
Tarp assisted cooling
Passive cooling
Arm Description
Whole body cooling in a small amount of 20'C water.
Supine lying
Outcomes
Primary Outcome Measures
Cooling Rate
Internal body temperature reduction throughout cooling
Secondary Outcome Measures
Full Information
NCT ID
NCT04095403
First Posted
September 13, 2019
Last Updated
February 14, 2022
Sponsor
State University of New York at Buffalo
1. Study Identification
Unique Protocol Identification Number
NCT04095403
Brief Title
Tarp Assisted Cooling of Hyperthermic Individuals
Official Title
Tarp Assisted Cooling of Hyperthermic Individuals
Study Type
Interventional
2. Study Status
Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
February 1, 2020 (Actual)
Primary Completion Date
February 14, 2022 (Actual)
Study Completion Date
February 14, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
State University of New York at Buffalo
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a randomized controlled trial exploring the difference in cooling rates between two treatments: 1) tarp-assisted cooling and 2) the standard of care for heat stroke treatment in the wilderness.
Detailed Description
This is a randomized controlled trial exploring the difference in cooling rates between two treatments: 1) tarp-assisted cooling and 2) the standard of care for heat stroke treatment in the wilderness. 12 healthy participants (6 males, 6 females) will participate. Visit 1 will be a screening visit, consisting of informed consent followed by completion of questionnaires to determine study eligibility. Participants will have their resting vital signs (heart rate, blood pressure), height, weight, and percent body fat measured. Visits 2 and 3 will be experimental trials. Participants will complete a treadmill protocol consisting of brisk walking wearing a weighted backpack (40 lb) until core temperature reaches 40.0°C. Upon completion of exercise, participants will exit the environmental chamber and be cooled in one of two ways in a randomized, counterbalanced manner: 1) tarp-assisted cooling or 2) Standard of Care. Cooling will take place for 20 minutes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy
Keywords
Heat, Cooling
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Randomized controlled trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Tarp assisted cooling
Arm Type
Experimental
Arm Description
Whole body cooling in a small amount of 20'C water.
Arm Title
Passive cooling
Arm Type
Sham Comparator
Arm Description
Supine lying
Intervention Type
Other
Intervention Name(s)
Tarp Assisted Cooling
Intervention Description
Body cooling utilizing a tarp and water
Intervention Type
Other
Intervention Name(s)
passive cooling
Intervention Description
Supine rest.
Primary Outcome Measure Information:
Title
Cooling Rate
Description
Internal body temperature reduction throughout cooling
Time Frame
20 minutes post-exercise.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
39 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy
Aerobic exercise at least twice weekly
Exclusion Criteria:
History of exertional heat illness
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Riana R Pryor, PhD
Organizational Affiliation
University at Buffalo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Research and Exercise in Special Environments
City
Buffalo
State/Province
New York
ZIP/Postal Code
14214
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Aggregate data can be shared upon request.
Learn more about this trial
Tarp Assisted Cooling of Hyperthermic Individuals
We'll reach out to this number within 24 hrs