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Clinical Trials in the USA / NCT05955482
Active, not recruiting Observational

Pragmatic Assessment of the NuvoAir Clinical Service in the Management of Patients With Chronic Obstructive Pulmonary Disease

NCT05955482 · tracked via the Priya Life Science USA tracker
Sponsor
NuvoAir Medical PC
Phase
Observational
Started
2023-07-24
Last updated
2025-05-28

Condition(s) studied

COPDComorbidities and Coexisting Conditions

Investigational drug(s) / intervention(s)

NuvoAir Clinical Service

NuvoAir Clinical Service: The NuvoAir clinical service offers comprehensive monitoring of health parameters and patient-reported outcomes as well as personalized clinical and behavioral interventions tailored to the patients' unique needs and their clinical risk. Furthermore, it involves virtual interaction with a NuvoAir Coach who provides guidance and assistance in navigating and utilizing the service. A dedicated NuvoAir care coordinator is available to offer self-management support and educational resources, aiming to enhance the management of COPD and other comorbidities. In situations where patients encounter new or worsening symptoms, the NuvoAir clinical team is accessible to provide medical intervention, advice and triage as required.

Study summary

This is a 12 month study of up to 500 people with COPD to determine if the NuvoAir clinical service leads to lower rates of severe COPD exacerbations, hospitalizations, emergency room visits, and total cost of care compared to a similar group that doesn't receive care from the NuvoAir clinical service.

Eligibility

Sex
ALL
Min age
30 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Have COPD, including emphysema and chronic bronchitis, per relevant COPD diagnostic codes in the past 2 years * Are age ≥30 years * Have access to a smartphone, cell phone, or landline telephone Exclusion Criteria: Do not have serious medical illness that would interfere with cooperation or understanding of instructions, including terminal illness, active substance abuse, or unstable mental illness or psychiatric condition * Does not have severe uncompensated heart failure, acute cor pulmonale, clinically unstable pulmonary embolism, history of syncope related to forced expiration/cough, cerebral aneurysm, presence of pneumothorax. * Is not pregnant or known intention to become pregnant within 12 months

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Marshfield Clinic Research Institute Marshfield Wisconsin

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05955482 on ClinicalTrials.gov ↗ ← All trials in the USA