A Novel Cooling Vest to Protect Persons With SCI From Hyperthermia
Spinal Cord Injuries
About this trial
This is an interventional device feasibility trial for Spinal Cord Injuries focused on measuring Body Temperature Regulation, Hyperthermia, Body Temperature
Eligibility Criteria
Inclusion Criteria:
- Spinal cord injury (SCI) >1 year in duration
- Level of SCI C4-T2, ASIA Impairment Scale A & B
- Gender and age-matched (±5 years) able-bodied (AB) controls
- Euhydration (participants will be instructed to avoid caffeine and alcohol, maintain normal salt and water intake and avoid strenuous exercise for 24 hours prior to study)
Exclusion Criteria:
- Known cardiovascular, kidney or untreated thyroid disease
- Traumatic brain injury (mod-severe)
- Diabetes mellitus
- Acute illness or infection
- Broken, inflamed, or otherwise fragile skin
- Pregnancy
- BMI >30 kg/m2
- Smoking Participants with SCI only (secondary to telemetry capsule (CorTemp®) measurement of Tcore)
- Undergoing magnetic resonance imaging while the telemetry capsule is within the body (2-5 days)
- Cardiac pacemaker or other implanted electromedical device
- Known or suspected obstructive disease of the GI tract
Sites / Locations
- James J. Peters VA Medical Center, Bronx, NY
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
No Intervention
Arm 1: Cooling Vest
Arm 2: Cooling Vest
Arm 3: No Vest
Phase 1: After satisfying bench testing criteria, AB participants will wear the wet cooling vest at maximal settings for 2 hours in the seated position in a warm thermal chamber (35°C), to determine: (1) minimum skin temperatures beneath the cooling vest and (2) subjective thermal sensation of their skin beneath the cooling vest.
Phase 2: Participants with Hi-SCI will wear the wet vest (experimental condition) in a warm thermal chamber (35°C) for up to 2 hours in the seated position, to determine: (1) change in Tcore and (2) perception of heat and thermal comfort.
Phase 2: Participants with Hi-SCI will wear no vest (control condition) in a warm thermal chamber (35°C) for up to 2 hours in the seated position, to determine: (1) change in Tcore and (2) perception of heat and thermal comfort.