Rebecca Borton

Jun 27, 2024 | bmjopenrespres.bmj.com | Sarah Barth |Colin Edwards |Rebecca Borton |Dan Beever

The study design is an unblinded randomised control study with parallel arms where participants will be randomly allocated (1:1) to either the remote monitoring arm or usual care arm. Following informed consent, baseline clinical data collected as part of usual clinical National Health Service (NHS) care will be used for the purpose of the study including previous medical history, all medication usage, previous lung function tests and radiology results.