Monitoring vital signs of emergency responders in various conditions
Vital Signs Monitoring of Emergency Responders in Different States
This study is testing how the vital signs and behaviors of emergency responders change when they're resting, after working, or after training in different environments to better understand their health.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 135 (estimated) |
| Ages | 20 Years to 45 Years |
| Sex | All |
| Sponsor | Qilu Hospital of Shandong University Academic / other |
| Locations | 1 site (Jinan, Shan Dong) |
| Trial ID | NCT06076057 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather data on the vital signs and behavioral parameters of emergency responders under different states, such as resting, post-duty, and after physical training. It will assess ten vital signs including respiratory rate, pulse rate, and oxygen saturation, as well as behavioral parameters like body position and muscle activity. Additionally, the study will evaluate vital signs in various environments, including altitude and confined spaces, to understand how these factors affect emergency responders' health. The data collected will help in understanding the physiological responses of responders in diverse situations.
Who should consider this trial
Good fit: Ideal candidates for this study are emergency responders without a history of significant cardiovascular or respiratory conditions.
Not a fit: Patients with severe heart disease, arrhythmias, or other significant health issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the health monitoring and safety protocols for emergency responders.
How similar studies have performed: While similar studies have been conducted, this specific approach to monitoring vital signs in emergency responders across various states and environments is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * No history of coronary heart disease, hypertension, asthma, upper respiratory tract infection, decompression sickness, or anemia. Voluntarily participated in this study and signed an informed consent form Exclusion Criteria: * Patients with severe heart disease and arrhythmia; patients with vital organ failure; patients with significant generalized edema; patients with dermatologic disease and generalized skin breakdown; and patients with vascular disorders of the limbs.
Where this trial is running
Jinan, Shan Dong
- Qilu Hospital of Shandong University — Jinan, Shan Dong, China (Recruiting)
Study contacts
- Study coordinator: Ma dedong
- Email: ma@qiluhuxi.com
- Phone: 18560082806
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.