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Heart Rate Variability and Stress Management Enhancement

J

Joseph Maroon

Status

Terminated

Conditions

Heart Rate Variability
Stress

Treatments

Device: Apollo Wearable Device

Study type

Interventional

Funder types

Other

Identifiers

NCT04381182
STUDY19020291

Details and patient eligibility

About

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.

Enrollment

20 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Neurosurgical Resident (UPMC)

Exclusion criteria

  • None

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Biostrap/Apollo Device Use
Other group
Description:
Participants wear a Biostrap wearable device which measures steps, heart rate, heart rate variability, sleep metrics, and quantitative data in typical day-to-day activities of residents. Participants then again wear Biostrap except now also with the Apollo device which is worn around the ankle and is suggested to modulate heart rate variability and perceived stress of participants.
Treatment:
Device: Apollo Wearable Device

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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