Apollo Remote Observational Sleep Study

Status Enrolling by invitation

Clinical Trial Summary

The purpose of this study is to examine how Transcutaneous Vibratory Stimulation (TVS) produced by the Apollo wearable affects sleep and cardiovascular function in a diverse real-world population of Apollo users.

Clinical Trial Description

The Apollo wearable is a consumer wellness device that offers a non-invasive, non-habit-forming wearable solution to improve performance and recovery under stress in children and adults by delivering gentle wave-like vibrations (Transcutaneous Vibratory Stimulation) to the body. In this observational cohort study, we will assess sleep and cardiovascular metrics measured during sleep by Oura ring in participants who use Apollo wearable device both historically (2 years in the past) as well as in the future (two years forward). Participants will not be required to make any changes to their activities of daily living or lifestyle except for the continued use of their Apollo wearable devices and answer periodic questionnaires through an online survey tool. Participant data for days with and without using the Apollo wearable will be analyzed to identify the near term and long term effects of using a TVS device on sleep and cardiovascular signatures. Environmental and confounding data will be derived from the survey data and biometrics data from the wearables. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05260489
Study type	Observational
Source	Apollo Neuroscience, Inc.
Contact
Status	Enrolling by invitation
Phase
Start date	January 18, 2022
Completion date	October 1, 2025

View Details

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