Clinical trials: Heart Rate Monitoring
Resident Wellness, Resident Burnout
Remote Physiologic Monitoring of Resident Wellness and Burnout
Resident wellness and physician burnout are under the spotlight more and more as data begins to show that there is a point of diminishing return on the number of hours in training.
- Conditions
- Resident Wellness, Resident Burnout, Sleep, Stress
- Trial name
- NCT04304703
- Testing
- WHOOP strap 3.0
- Where
- United States
- Volunteers
- 38 people, healthy volunteers welcome
- Sponsor
- Milton S. Hershey Medical Center
Infant Development
A Pilot Study Using Photo-plethysmographic (PPG) Camera
The researcher want to use video signals to monitor heart rate, respiration rate and oxygen saturation using Photo-plethysmography (PPG) as the underlying mechanism for the method: periodic changes in skin reflectance, induced by…
- Trial name
- NCT01166867
- Testing
- Photo-plethysmography monitoring
- Where
- United States
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- University of California, Irvine
Burnout, Sleep Disturbance
Non-Invasive Sleep Monitoring for Burnout and Retention Risk in Postgraduate Nurses
Newly graduated nurses often experience high levels of psychological stress, sleep disturbance, fatigue, and burnout during the early transition into clinical practice.
- Conditions
- Burnout, Sleep Disturbance, Occupational Stress, Mental Health
- Trial name
- NCT07666633
- Testing
- Non-Invasive Sleep Monitoring
- Where
- Taiwan
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Kaohsiung Armed Forces General Hospital
Pregnancy
Fetal Pulse Oximetry Trial (FOX)
The purpose of this study is to determine if the information provided to the physician by a fetal pulse oximeter during labor will reduce the chances of a cesarean delivery.
- Trial name
- NCT00098709
- Testing
- Fetal pulse oximeter
- Where
- 13 sites in United States
- Volunteers
- 10,000 people, healthy volunteers welcome
- Sponsor
- The George Washington University Biostatistics Center
Diabetes
Distinguishing Participant Groups Using Autonomic Dysfunction
A study population with impaired fasting glucose levels, impaired glucose tolerance levels and diabetes (with or without complications) along with healthy patients will be chosen as participants.
- Trial name
- NCT05199350
- Testing
- Device Name: ANSiscope
- Where
- India
- Volunteers
- 175 people, healthy volunteers welcome
- Sponsor
- DyAnsys, Inc.