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An Evaluation of Remote Care (questionnaire+hybrid) in Patients Who Are Post-lung Transplant

An Evaluation of Remote Care (questionnaire+hybrid) in Patients Who Are Post-lung Transplant

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05916495
Enrollment
100
Registered
2023-06-23
Start date
2023-09-29
Completion date
2025-12-31
Last updated
2024-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Transplant; Complications

Brief summary

Lung transplantation is used to treat patients with lung damage when there is no other treatment option. Patients require close monitoring following their transplant, with hospital check-ups every 3-4 months usually lasting all day. Although check-ups often result in no change to patient management they are essential as patients have better outcomes if complications are detected quickly. The aim is to explore whether remote monitoring via an app (patientMpower) ± questionnaire (specifically designed to assess post-transplant patients' health), linked to a device to measure lung function, could replace some check-ups for lung transplant patients. Patients will be randomised to receive either normal care or remote monitoring (i.e. their symptoms will be evaluated using home spirometry combined with a questionnaire). 100 lung transplant recipients will be enrolled with 50 patients being assigned to either group. Health outcomes and costs of care between the two groups will be compared

Detailed description

100 lung transplant patients are expected to be recruited. Consent will be taken by the research team. Following admission they will be randomised to the interventional or control arms. The control arm will consist of follow-up according to unit policy, in the majority of cases this will be every 3 months. The only change is that when they come to follow up the patients will be asked to fill in the same interventional questionnaire (designed to assess post-transplant lung health) that the interventional arm are completing. However, they will be seen regardless of what this questionnaire reports. This will act as validation for the questionnaire. The interventional arm will replace the 3 monthly visits with a questionnaire which the patient will be asked to complete and then this will be returned to the unit. The patient can fill this in via the app, or on paper and return the questionnaire via email or post. The duty clinician will then review the questionnaire and combine this with the home spirometry data which the patient is already completing to see if the patient needs to be seen. In the majority of cases, its expected that the patient will not need to be seen as the clinic visits in lung transplant are mainly monitored and the vast majority of the patients are seen every 3-4 months. Regardless of the outcome, the participant will receive a phone call from the transplant nurse within 48 hours of the appointment to discuss the results of the blood test and confirm that they are okay. In addition to the questionnaire to assess lung health, all participants will be asked to complete other respiratory/sleep questionnaires such as Saint George's Respiratory (SGRQ), Morningness-eveningness (MEQ-SA) and the Pittsburgh Sleep Quality Index (PSQI). This will investigate whether more complex questionnaires are needed to see if patients require clinical follow-up. Study duration is predicted to be 6 months per participant. During the whole study, volunteers will be asked to wear an activity tracker such as Fitbit. Using the device's application programming interface (API) investigators will be able to remotely access data concerning heart rate, accelerometry and sleep duration, including stages of sleep. This will be accessed as required anticipated to be once per week, followed by phone calls to patients should the data be missing. In addition, their clinical record will also be accessed to obtain clinical data for instance if a sleep study has been performed. Patients will be asked to perform daily home spirometry using a Bluetooth enabled spirometer. It is currently being used in the Manchester lung transplant program. If patients have not submitted a reading for one week then they will be contacted by the study team to offer assistance.

Interventions

OTHERHybrid care arm

Patients will be evaluated at 3 months via a remote review. This will review the patients-recorded spirometry and a questionnaire developed for this study which asses the patients' symptom burden and medication adherence. All patients participating in the study will be offered remote monitoring (patient facing app+ patient recorded home spirometry).

Patients will be reviewed in clinic at 3 months per the standard of care. All patients participating in the study will be offered remote monitoring (patient facing app+ patient recorded home spirometry).

Sponsors

patientMpower Ltd.
CollaboratorINDUSTRY
Manchester University NHS Foundation Trust
CollaboratorOTHER_GOV
University College, London
CollaboratorOTHER
New Start, The Wythenshawe Hospital Transplant Fund Centre
CollaboratorUNKNOWN
University of Manchester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Looked after by a clinical care team at Manchester University NHS Foundation Trust * Given consent * Have received a lung transplant

Exclusion criteria

* Consent not given * Not able to operate the remote monitoring platform

Design outcomes

Primary

MeasureTime frameDescription
Number of clinic visits per patient6 monthsThe number of clinic follow up visits in the observation period

Secondary

MeasureTime frameDescription
Number of unplanned clinic visits per patient6 monthsThe number of unplanned clinic visits in the observation period
Measuring the Utilization Rate of Remote Monitoring for Patient Engagement Measuring the Utilization Rate of Remote Monitoring for Patient Engagement Number of patient interactions with the remote monitoring platform6 monthsFrequency of use at ≥ 1 day/week
Number of planned clinic visits per patient6 MonthsThe number of planned clinic visits in the observation period
Duration of hospitalisations due to deterioration of allograft function6 MonthsNumber of hospitalised days due to deterioration of allograft function
Number of patients where symptoms were recorded accurately on the questionnaire6 monthsThe number of patients where a clinician recorded that symptoms were recorded accuratly
Hospitalisation due to deterioration of allograft function6 MonthsNumber of patients hospitalised due to deterioration of allograft function

Countries

United Kingdom

Contacts

Primary ContactRebecca Borton
researchoffice@patientmpower.com+442033224121

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026