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NCT04381182

Heart Rate Variability and Stress Management Enhancement

Terminated NA Last updated 6 December 2022
What this trial tests

NA trial testing Apollo Wearable Device in Stress in 20 participants. Terminated before completion.

Timeline
1 September 2021
Primary endpoint
20 July 2022
20 August 2022

Quick facts

Lead sponsorJoseph Maroon
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment20
Start date1 September 2021
Primary completion20 July 2022
Estimated completion20 August 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Joseph Maroon

Who can join

Eligibility, any sex, with Stress or Heart Rate Variability. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Stress

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04381182.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing