Musculoskeletal Disorders
Conditions
Interventions
Participants will wear a wearable device and Holter electrocardiography during endoscopic procedures to continuously measure physiological parameters, including heart rate variability.
Sponsors
Mie University Graduate School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Physicians, nurses, or clinical engineers working at our institution 2. Scheduled to be engaged in endoscopic procedures, including colonoscopy, ERCP, EUS-FNA, or ESD 3. Able to wear the measurement devices (wearable device and Holter electrocardiography) for a specified period 4. Provided written informed consent to participate in the study
Exclusion criteria
Exclusion criteria: 1. Individuals with cardiovascular disease or autonomic dysfunction that may affect heart rate variability assessment 2. Individuals who are regularly taking medications that affect heart rate or autonomic nervous system function 3. Individuals for whom wearing the measurement devices is difficult or inappropriate due to skin conditions or allergies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To quantitatively evaluate changes in physiological parameters, including heart rate variability, pulse wave, and acceleration, in healthcare providers during endoscopic procedures, as measured using wearable devices and Holter electrocardiography, by comparing values before, during, and after the procedures. | — |
Countries
Japan
Contacts
Public ContactAiji Hattori
Mie University Graduate School of Medicine Department of Gastroenterology and Hepatology
Outcome results
None listed