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Clinical Trial Summary

Develop an app-based nationwide study of individuals who routinely use a smartwatch or other wearable activity tracker to determine if individualized tracking of changes in heart rate, activity and sleep can provide an early indication of influenza-like illnesses (ILI) and possibly other viral infections.


Clinical Trial Description

This study will be configured in CareEvolution's myDataHelps platform. This app-based platform will allow people to: - Provide informed consent electronically - Donate robust smartwatch and activity tracker data, as well as self-reported data. - Sensor-collected data, which will vary between devices, but what is shared will always be entirely up to the participant. Investigators anticipate a minimum to include heart rate and activity, plus sleep duration when available. - This can include historical data collected by a sensor prior to the participants date of joining the study. - Occasional survey-based participant-reported outcomes (PROs). - Participant-entered physiologic data such as oral temperature - Passively share environmental data such as air quality and weather that will be captured from external sources based on participants' "home" zip code. Optionally, if the participant consents to enable location/GPS services on their smartphone, higher grain environmental data will be enabled. - Optionally connect to and share their electronic health record (EHR) data in the event they have an event that requires interaction with a health care provider ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04336020
Study type Observational
Source Scripps Translational Science Institute
Contact Lauren Ariniello, BS, CCRC
Phone 858.784.2253
Email laurena@scripps.edu
Status Recruiting
Phase
Start date March 24, 2020
Completion date April 2025

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