Clinical trial Recruiting at 1 site Interventional Ages 18 and up

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 typeInterventional
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorUniversity of Pittsburgh
Academic / other
Locations1 site (Pittsburgh, Pennsylvania)
StatusRecruiting
StartedJanuary 15, 2024
Main results expectedNovember 2027
Study endsNovember 2027
Registry record updatedFebruary 18, 2026
Trial IDNCT05731856 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

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.