Use of Technology and Telemedicine to Improve Quality of Care in COVID 19 Patients

Covid19 Clinical Trial

Official title:

Use of Technology and Telemedicine to Improve Quality of Care in COVID 19 Patients

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT04480411
• Other study ID #: 56472
• Status: Withdrawn
• Phase: N/A
• Start date: January 2022
• Est. completion date: December 2022

Study information

• Verified date: January 2022
• Source: Stanford University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the use of technology including remote vital sign monitoring in improving quality of patient care, decreasing hospital admissions and re-admissions, decreasing hospital length of stay and decreasing use of personal protective equipment.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2022
• Est. primary completion date: December 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Hospitalized patient with COVID 19 or outpatient under investigation for or diagnosed with COVID 19

• Clinically stable (on 4L O2 or less, non ICU)

• Demonstrates ability to be trained in use of digital stethoscope technology

Exclusion Criteria:

• Pregnancy

• Delirium

Related Conditions & MeSH terms

• COVID-19
• Covid19
• Diagnoses Disease

Intervention

Behavioral:
• Doctorgram Patient Kit
Participants will use the Doctorgram Patient Kit for remote monitoring and remote use stethoscope.

Locations

Country	Name	City	State
United States	Stanford University	Stanford	California

Sponsors (1)

Lead Sponsor	Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patient provider experience survey score	Five questions related to satisfaction with experience using home pulse oximetry, each on a scale of 1 (poor) to 5 (excellent) summed and averaged for an overall range of 1 to 5 (higher scores = better experience).	Once after completion of device use (up to 15 minutes to complete the survey)
Primary	Provider experience survey score	Four questions related to satisfaction with experience using home pulse oximetry, each on a scale of 1 (poor) to 5 (excellent) summed and averaged for an overall range of 1 to 4 (higher scores = better experience).	Once after completion of device use (up to 15 minutes to complete the survey)
Primary	Use of personal protective improvement	Level of personal protective improvement in an in-patient setting.	6 months
Primary	Number of in-patient encounters with COVID patients as a measure of provider exposure to high risk illness		6 months