Table 1

Trial schedule of events and data collection

Before randomisationBaseline+randomisationIntervention group6 months
RemoteFace to faceRemote by AcurableRemote
Identification of eligible patients (inclusion/exclusion criteria)✓
Invitation to participate in study✓
Written and witnessed informed consent✓
Collection of questionnaires (Clinical and Health Economics)✓✓
Randomisation✓
Delivery of AcuPebble✓
Analysis of OSA test and reporting outcome✓
Primary outcome✓
Secondary outcomes✓

  • OSA, obstructive sleep apnoea.