Heart Rate Variability and Stress Management Enhancement
Burnout, Professional
About this trial
This is an interventional supportive care trial for Burnout, Professional
Eligibility Criteria
Inclusion Criteria: UPMC attending physicians and residents. The participants must have either IOS or Android phones. Exclusion Criteria: Unwillingness or inability to participate in the study Currently own an Apollo device
Sites / Locations
- University of Pittsburgh
Arms of the Study
Arm 1
Experimental
Apollo Intervention Arm
Eligible UPMC Physicians and Residents who consent to be part of this study will use an Apollo Device TVS (10-200 Hz) attached to the subject's wrist or ankle via a commercially available wearable vibration technology that can deliver TVS (Transcutaneous Vibratory Stimulation). The intensity will be targeted for the sensory threshold (the level at which the vibration is just noticeable), as this is where the TVS seems most effective from prior studies. Similar vibratory stimuli have been demonstrated to be safe in the literature. The intensity of the vibration will be adjusted to the subjects' comfort and can be controlled by the subject at any time.