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Clinical Trial Summary

The ALPACA study has a prospective randomized control interventional design, including a follow-up period to evaluate follow-up effects. The study is divided into two phases of 3 months using eHealth and observational monitoring.


Clinical Trial Description

The ALPACA study has a prospective randomized control interventional design, including a follow-up period to evaluate follow-up effects. The study is divided into two phases of 3 months; In the first phase subjects are randomized to either eHealth care (use of a communication portal including the weekly entry of SpO2, spirometry results and ACT) and explorative observational home-monitoring or only explorative observational home-monitoring during regular care. The second phase is to evaluate the effects of eHealth care compared to the control group after a follow-up period of 3 months, and the time to healthcare events during follow-up in both groups (survival analysis). The study makes use of an intention-to-treat analysis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05517096
Study type Interventional
Source Philips Electronics Nederland B.V. acting through Philips CTO organization
Contact I Geven, master Science
Phone +31646545735
Email inge.geven@philips.com
Status Recruiting
Phase N/A
Start date October 7, 2022
Completion date March 1, 2024

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