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Heart Rate Variability and Stress Management Enhancement

NCT04381182 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2022-12-06

No results posted yet for this study

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.

Conditions

  • Stress
  • Heart Rate Variability

Interventions

DEVICE

Apollo Wearable Device

Participants wear Apollo device which generates vibration frequencies on skin and can be controlled by the user

Sponsors & Collaborators

  • Apollo Neuro

    collaborator UNKNOWN

  • Joseph Maroon

    lead OTHER

Principal Investigators

  • Joseph Maroon · Department of Neurological Surgery

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-01
Primary Completion
2022-07-20
Completion
2022-08-20

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04381182 on ClinicalTrials.gov