Simulation of Consecutive Day Shift Work
- Conditions
- HyperthermiaFatigue; Heat
- Interventions
- Other: 2 days of work heat stress
- Registration Number
- NCT04625634
- Lead Sponsor
- State University of New York at Buffalo
- Brief Summary
The purpose of this study is to determine differences in physiological recovery between two consecutive days of simulated fire suppression work. The secondary purpose is to determine differences in heat gain and heat loss between two consecutive days of simulated fire suppression work. Subjects will complete two consecutive days of simulated structural firefighting shift work, 24 hours apart. Before and after each laboratory visit, subjects will continuously wear a Holter monitor and ambulatory blood pressure monitor to quantify parasympathetic tone and recovery from work.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 23
- 18-39 y old men and women
- Self-reported to be healthy
- History of any cardiovascular, neurologic, renal, or metabolic disease
- Current tobacco use or regular use within the last 2 years
- Taking medications with known thermoregulatory or cardiovascular effects (e.g., aspirin, acetaminophen, ibuprofen, beta blockers, diuretics, psychotropics, etc.)
- History of exertional heat stroke
- Currently pregnant or breastfeeding, or planning to become pregnant during the study
- Inability to follow the rules of the protocols or understand the consent form
- No contraindications for ingestion of the gastrointestinal temperature pill
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Consecutive work 2 days of work heat stress Subjects will complete 2 consecutive days of simulated firefighting tasks in the heat. The simulated work consists of 20 minutes of simulated structural work in a hot environment, followed by 20 minutes of seated rest in a temperate room, mimicking a typical recovery period in structural firefighting. Subjects then re-enter the environmental chamber and complete 23 minutes of simulated overhaul work in a temperate environment.
- Primary Outcome Measures
Name Time Method Core temperature 20 minutes Gastrointestinal temperature measured with an ingestable pill.
Heart rate 20 minutes Heart rate measured with a wearable heart rate strap and monitor
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Center for Research and Exercise in Special Environments
🇺🇸Buffalo, New York, United States