The COPD CARE Study: Evaluating the Impact of a Virtual-First COPD Service on Major Cardiac and Respiratory Events

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-100
SponsorNuvoAir Medical PC

About this trial

A 12 month interventional study of up to 1,050 people with COPD to determine if the NuvoAir virtual-first clinical service leads to fewer moderate and severe COPD exacerbations and cardiac events, reduces healthcare utilization, and lowers the total cost of care compared to a control cohort that receives standard care only.

Eligibility criteria

Qualifiers

Twelve months of claims data in the health insurer or provider's database for baseline

ICD10 code for COPD (including emphysema and chronic bronchitis) with a severe exacerbation of COPD in the previous 12 months (defined as ER visit or hospitalization related to COPD or severity score of 2 or 3)

Cooperative, i.e., subject should be able to follow and understand instructions

Access to a phone (smartphone, cell phone, or landline)

Disqualifiers

Does not have access to a a phone (smartphone, cell phone, or landline)

Lack of cooperation, subject cannot follow and understand instructions

Other serious medical illness that, in the opinion of the PI, would interfere with the patient's participation in the study or interpretation of their data (i.e., terminal illness, unstable psychiatric condition, etc.)

Does not understand English

Trial design

Treatments tested in this trial

  • NuvoAir clinical service

Treatment groups

1,050 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

NuvoAir Medical PC

Lead sponsor

Optum, Inc.

Collaborator