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A Real-World Assessment of a COPD Disease Management Support Service (Me & My COPD)

A Real-World Assessment of a COPD Disease Management Support Service (Me & My COPD).

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02300090
Acronym
Me&MyCOPD
Enrollment
161
Registered
2014-11-24
Start date
2016-10-26
Completion date
2018-08-23
Last updated
2018-09-11

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

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

COPD, Exacerbation, respiratory disease, lung disease, breathlessness, dyspnoea, sputum, wheezing, cough

Brief summary

A real world study to determine the effectiveness of a patient support service to aid COPD patients in their self management.

Detailed description

The purpose of the study is to evaluate a digital health wellness support tool for patients in primary care with COPD using a smart mobile app, patient web portal and technology attached to the patients SABA reliever inhaler. Using the patients pre-defined COPD self management plan, the active arm of the study complete a daily diary (EXACT PRO) and record their daily SABA inhaler usage. After defining a health and symptom score baseline over a two week period, any significant deviations in SABA reliever use or daily diary scoring will alert patients that they may be having a change in their symptoms and advise them to refer to their self management plan and if they need to start their rescue medication. The primary outcome measure for the study is a 25% reduction in unplanned COPD hospital admissions (n=250 completing the study in each arm).

Interventions

Patients receive a mobile phone with the Me & My COPD app installed. Patients also receive a bluetooth inhaler device that is fitted to their usual reliever inhaler.

OTHERControl Group

Patients in the control group receive only standard care; there are no interventions within this group of patients

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of COPD * FEV1/FVC ratio \>0.3-\<0.7 and FEV1 \> 30% post-bronchodilator * Prescribed either ICS, LABA and or LAMA at dose for COPD * Exacerbations reported within the last 12 months requiring treatment with \>1 systemic steroid and/or antibiotics, OR hospitalisation within last 12 months due to exacerbation, OR have received \>12 SABA prescriptions in previous 12 months * Patient has a self management plan which includes use of an oral steroid at a dose within NICE guidelines, and additionally antibiotics as appropriate.

Exclusion criteria

* Symptomatic asthma or seasonal allergic rhinitis leading to hospitalisation in previous 12 months * Patients unable to use a mobile phone

Design outcomes

Primary

MeasureTime frameDescription
To detect a reduction in the rate of hospitalisations due to COPD exacerbationsAnalysed over a twelve month timeframeThe mean number of COPD related hospitalisations per patient per year for patients who are receiving the digital service in the study will be compared to the rate of COPD related hospitalisations in patients receiving current best care alone over a twelve period.

Secondary

MeasureTime frameDescription
To detect a reduction in the duration of hospitalisations due to COPD exacerbations.12 monthsThe average duration of COPD related hopspitalisations (number of bed days) per patient will be compared across patients receiving the digital service and those receiving current best care alone.
To detect a reduction in the number of exacerbations requiring treament with antibiotics and or systemic steriods12 monthsThe number of exacerbations requiring treament with antibiotics and or systemic steriods will be compared across patients receiving the digital service and those receiving current best care alone.
To detect an improvement in patients own perceived health status, as assessed by St Georges Respiratory Questionnaire-C12 monthsThe patients assessment of their own health status will be assessed over time using the St Georges Respiratory Questionnaire-C, and will be compared across patients receiving the digital service and those receiving current best care alone.

Other

MeasureTime frameDescription
To detect a difference in the use/prescribing of reliever therapy12 monthsTo detect a difference in the use/prescribing of reliever therapy, as measured through repeat prescriptions, by comparison of patients receiving the digital service and those receiving current best care.
To assess patinet engagement in the use of the digital service12 monthsTo assess the engagement of patients receiving the digital service as measured by frequency of access to infromational content and goal management.
To detect a difference in the use/prescribing of maintenance therapy12 monthsTo detect a difference in the use/prescribing of maintenance therapies (inhaled corticosteroids/long acting beta agonists and or long acting muscarinic antagonists) by comparison of repeat prescriptions across patients receiving the digital service and those receiving current best care alone.

Countries

United Kingdom

Outcome results

None listed

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