About this trial

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.

Eligibility criteria

Qualifiers

Age 18-30;

In good health, with no history of cardiovascular disease, respiratory disease, diabetes, endocrine disorders, neurological or psychiatric conditions;

No smoking or alcohol addiction, no history of substance abuse;

No prior history of particular sensitivity to high-temperature environments.

Disqualifiers

Individuals who have experienced fever, colds, infectious diseases, or significant physical trauma within two weeks prior to the high-temperature test;

Individuals currently using medications that may affect psychological, cognitive, cardiovascular, or respiratory functions;

Pregnant women and lactating females;

Participants shall not be scheduled to participate during menstruation;

Trial design

Treatments tested in this trial

  • Daytime or Nighttime High-Temperature Exposure
  • Daytime and nighttime neutral temperature exposure

Treatment groups

35 Participants
are divided into 2 treatment groups

Locations

1
Anhui Medical University230032, HefeiAnhui, China

Sponsors and collaborators

Jian Cheng

Lead sponsor

Anhui Medical University

Sponsor institution