Home Pulse Oximeter Use in Patients With COVID-19

Swedish Hospital

Status: Completed

Conditions: COVID-19; Sars-CoV2; COVID

Treatments: Device: Home Pulse Oximetry Monitoring

Study type: Interventional

Funder types: Other

Identifiers

NCT04373161

2020032301

Details and patient eligibility

About

The purpose of this study is to investigate the use of home pulse oximetry monitoring in patients with COVID-19 to trend disease progression and identify need for hospitalization.

Full description

This protocol studies patients with suspected non-severe Corona Virus Disease (COVID-19) being discharged to home from an emergency department (ED) or outpatient testing center. Patients will be provided a portable fingertip home pulse oximeter that measures peripheral oxygen saturation (SpO2). Patients will be instructed to check their resting home oxygen saturation three times per day and record these findings. They will be instructed to return to the emergency room for sustained oxygen saturation below 92% or if their symptoms are worsening and they feel they need medical attention. Patients will be called once daily by the research team to collect data in real time. Patients will be monitored for seven days, and at the end of the seven day period, they will return the pulse oximeter as well as a spreadsheet of their home oximetry readings. The purpose is to see if home pulse oximetry identifies disease progression and need for hospitalization in patients with COVID-19. Additionally, there will be analysis of trends in home oximetry readings wand predictors of morbidity and mortality.

Enrollment: 209 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with suspected COVID-19 as defined by the World Health Organization
• Age > 18

Exclusion criteria

• Pregnancy
• Prisoners
• Lack of decision making capacity or cannot provide consent
• Patients being admitted to the hospital
• Patients on home oxygen
• Patients being discharged to a skilled nursing facility

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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209 participants in 1 patient group

Suspected COVID-19 patients being discharged to home

Experimental group

Description:

Patients will be given a portable, fingertip pulse oximeter to take home. Patients will monitor their resting home oxygen saturation three times per day.

Treatment:

Device: Home Pulse Oximetry Monitoring