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Clinical Trial Summary

This study will be conducted by using two devices (Apollo and Biostrap) for monitoring of baseline physiologic variables and heart rate variability. The biostrap will be worn by residents and will monitor heart rate, heart rate variability, respiratory rate, sleep patterns, steps, etc. The Apollo is a pulse generator device aimed at modulating heart rate variability for (hopefully) reduction in stress and improving performance in and around the hospital. Resident neurosurgeons will wear the biostrap for a two week cycle and follow that with the addition of the Apollo device for heart rate variability modulation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04381182
Study type Interventional
Source University of Pittsburgh
Contact
Status Terminated
Phase N/A
Start date September 1, 2021
Completion date August 20, 2022

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