Clinical study analyzes correlation between body temperature and related symptoms among workers in hot work environments
- Conditions
- Not Applicable
- Registration Number
- KCT0009572
- Lead Sponsor
- Cheonan Korean Medicine Hospital of Daejeon University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 10
1) Adult men and women 19 years of age or older and up to 64 years of age
2) People who work in occupations where exposure to heat illness is frequent
(e.g., sales and service workers, construction workers, factory workers, mechanics, repairmen, security personnel, food service workers, agricultural workers, workers in high-temperature work environments such as foundries, furnace operators, crack furnace operators, construction machine operators, ceramics and glassware manufacturers, etc.)
3) Those who can be followed up during the test period
4) Those who voluntarily decide to participate in the clinical study after being fully informed about the purpose, content, and characteristics of the study before participating in the study and give written consent.
1) History of severe migraine, diagnosed thromboembolism, cerebrovascular disease, myocardial infarction, unstable angina, or coronary angioplasty within one year of screening
- Have at least 5 or more headache episodes; headache duration of 4 to 72 hours; unilateral, moderate, or severe pain intensity; pulsatility; headache worsening with activities of daily living; and comorbid symptoms such as nausea and vomiting, light or sound phobia
2) Have a history of uncontrolled hypertension.
- Resistant hypertension in which blood pressure is not controlled to 140/90 mm Hg or less despite adequate and appropriate administration of three or more medications, including diuretics
3) History of alcohol or drug abuse
4) Unable to complete patient-completed measures on their own or with guardian/investigator assistance
5) Participated in another clinical study and received an intervention within 4 weeks of the screening visit for this study
6) deemed by the investigator to be inappropriate for participation in this study
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method