Using a gentle wearable to reduce stress and burnout in physicians
Official title: Impact of Heart Rate Variability Modulation on Stress and Recovery Among Physicians
Run by University of Pittsburgh · NCT05731856 · Data updated 2026-11-12
This will test whether wearing the Apollo device's gentle vibrations can reduce burnout and improve stress recovery for physicians.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | University of Pittsburgh Academic / other |
| Locations | 1 site (Pittsburgh, Pennsylvania) |
| Status | Recruiting |
| Started | January 15, 2024 |
| Main results expected | November 2027 |
| Study ends | November 2027 |
| Registry record updated | February 18, 2026 |
| Trial ID | NCT05731856 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are UPMC attending physicians or residents who have an iOS or Android phone, do not already own an Apollo device, and are willing to wear the device and complete questionnaires.
✕Probably not a fit
Physicians who already own an Apollo device or who are unwilling or unable to wear the device or complete study procedures would not gain benefit from participation in this protocol.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The study uses a Tuned Vibroacoustic Stimulation device (the Apollo wearable) that produces low-volume sound waves felt as a soothing touch to the skin to modulate heart rate variability (HRV). Physicians at the University of Pittsburgh (UPMC attendings and residents) will wear the Apollo device during work and recovery periods and complete questionnaires before and after use. The protocol compares self-reported stress and recovery measures alongside HRV modulation produced by the device. The goal is to determine whether small HRV changes translate into reduced burnout and faster stress recovery in and around the hospital.
Why it matters
Potential benefit: If successful, the wearable could offer a non-drug way to lower burnout symptoms and speed recovery from stress for physicians.
How similar studies have gone: Prior clinical studies at the University of Pittsburgh have shown the Apollo device can improve heart rate variability and recovery under stress, so this applies that approach to physician burnout.
Who can join: the full rules
Show full inclusion / exclusion 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
Where it's running
-
University of Pittsburgh
Pittsburgh, Pennsylvania, United States Recruiting
Study contacts
- Principal investigator: Michelle Thompson, DO — University of Pittsburgh
- Study coordinator: Franchesca Inay, BS
- Email: inay.franchesca@medstudent.pitt.edu
- Phone: 5512234990
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.