Assess the acute effects of high-temperature exposure (including both daytime and nighttime conditions) on multiple physiological and psychological indicators, including cardiovascular, respiratory, neuropsychiatric, and metabolic functions, along with their potential mechanisms.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Heart Rate Variability
Timeframe: Volunteers will be asked to wear smart band for 24 hours from 6:00 A.M. at the day of intervention to 6:00 A.M. at the next day.
Systolic and Diastolic Blood Pressure
Timeframe: Blood pressure will be examined before exposure and immediately (within 10 mins) after the exposure session
Forced Expiratory Volume in 1 Second
Timeframe: Lung function will be examined before exposure and half an hour after the exposure session
Forced Vital Capacity
Timeframe: Lung function will be examined before exposure and half an hour after the exposure session
Interleukin-6
Timeframe: Blood will be collected 1 hour before and after the exposure session
C-reactive Protein
Timeframe: Blood will be collected 1 hour before and after the exposure session
F2-Isoprostanes
Timeframe: Blood will be collected 1 hour before and after the exposure session
Superoxide Dismutase
Timeframe: Blood will be collected 1 hour before and after the exposure session
Serum Creatinine
Timeframe: Blood will be collected 1 hour before and after the exposure session
Urinary Neutrophil Gelatinase-Associated Lipocalin
Timeframe: Urine will be collected 1 hour before and after the exposure session
Profile of Mood States
Timeframe: Scale assessments will be conducted within one hour before and after exposure.