Detection of COVID-19 Decompensation

Completed

Conditions studied: Covid19

In brief

In this study we will be monitoring for patient events (emergency department admission, hospital admission, admission to an observation unit, or death) and evaluating the feasibility and utility of using pinpointIQ in the management of patients with COVID-19. Vital sign (physiology data) is collected to build a Covid Decompensation Index and contribute data to a Covid Digital Hub supported by the National Institutes of Health.

Key facts

Study ID

NCT04575532

Run by

physIQ, Inc.

People needed

1000

Starts

2020-10-05

Expected to finish

2021-09-09

Last updated by the study team

2021-09-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Obtained signed and dated informed consent form Patient in the University of Illinois Health System Patient agrees to comply with all study procedures and availability for the duration of the study Male or female, aged > 18 years of age Patient diagnosed with COVID-19 (positive SARS CoV2 test) Patient agrees to refrain from swimming or taking baths (any activity that submerges the biosensor in water for any period). Showering is okay.

You may not qualify if…

• Known allergic reactions to components of the hydrocolloid gel adhesives Subject has cognitive or physical limitations that, in the opinion of the investigator, limits the subject's ability to fully follow study procedures Cognitive ability, in the opinion of the investigator, that limits the patient's ability to use the biosensor and smartphone consistent with study requirements.
• Does not speak or read English or Spanish

Where it is running

• Rush University Medical Center — Chicago, Illinois, United States
• University of Illinois Hospital and Health Sciences System — Chicago, Illinois, United States
• NorthShore University HealthSystem — Evanston, Illinois, United States
• University of Texas Health — Houston, Texas, United States

Full record on ClinicalTrials.gov

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