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Trials / Completed

CompletedNCT05259280

Observational Study of the Wellinks Solution Impact on Quality of Life and Clinical Outcomes in Patients With COPD

ASPIRE: An Observational Study of the Wellinks Solution Impact on Quality of Life and Clinical Outcomes in Patients With COPD

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
153 (actual)
Sponsor
Convexity Scientific Inc · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The clinical objectives of this study are to determine whether utilization of the Wellinks COPD Solution can improve quality of life for patients with COPD, can reduce healthcare resource utilization over time, and can improve pulmonary function as measured by connected devices. The nonclinical objectives of this study are to describe the experience of patients using the Wellinks Solution through the assessment of patient engagement with the solution, as well as by patient-reported satisfaction with the solution and their perceived value (e.g., willingness to pay). Qualitative feedback on the features and functionality of the Wellinks Solution will be solicited.

Conditions

Interventions

TypeNameDescription
OTHERWellinksDigital health and virtual care program for COPD management.

Timeline

Start date
2022-01-05
Primary completion
2022-09-08
Completion
2022-09-08
First posted
2022-02-28
Last updated
2023-11-02

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT05259280. Inclusion in this directory is not an endorsement.

Observational Study of the Wellinks Solution Impact on Quality of Life and Clinical Outcomes in Patients With COPD (NCT05259280) · Clinical Trials Directory