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UnknownNCT05299372

Telemonitoring in NIV MND (OptNIVent)

Optimising the Management of Ventilated Patients and Quality of Life in Motor Neurone Disease: a Pilot Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
15 (estimated)
Sponsor
Liverpool University Hospitals NHS Foundation Trust · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHERTelemonitoring via Careportal®The question sets and overnight oximetry results will be monitored and screened by a call centre commissioned by the Liverpool Clinical Commissioning Group (LCCG). The call centre will screen the weekly data and contact clinicians where appropriate (i.e. NIV team, MND specialist nurse, or patient's GP). PVI data will be examined by NIV physiotherapists, where required, following the contact from LCCG to ensure the maximum benefits of NIV to patients.

Timeline

Start date
2022-04-25
Primary completion
2022-10-31
Completion
2022-12-31
First posted
2022-03-29
Last updated
2022-03-29

Source: ClinicalTrials.gov record NCT05299372. Inclusion in this directory is not an endorsement.