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Clinical Trial Summary

This is a feasibility study of telemonitoring system for people with MND/ALS, who are on NIV, via a call centre operated by a local clinical commissioning group.


Clinical Trial Description

This study will test the feasibility of previously developed Telehealth system, using a device called Careportal®, to monitor people with MND/ALS who are using non-invasive ventilation (NIV). The Careportal® is a CE marked portable tablet computer device allowing telecommunication between patients and their care team through bespoke question sets, overnight oximetry test, and patient-ventilator interaction(PVI) data. Previously, the weekly telemonitoring via Careportal® was found to be an effective method to monitor symptom changes, allowing clinicians to optimise the care of ventilated patients with MND. This study will assess the practicality of using Careportal® in the care of ventilated patients with MND by monitoring patients through a patient support call centre. The call centre will screen the data and liaise with appropriate clinicians regarding changes of symptoms. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05299372
Study type Interventional
Source Liverpool University Hospitals NHS Foundation Trust
Contact Hikari Ando, PhD
Phone 0151529
Email hikari.ando@nhs.net
Status Not yet recruiting
Phase N/A
Start date April 25, 2022
Completion date December 31, 2022

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