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Evaluation of myAirCoach self-management support compared with usual care in asthma: a pragmatic randomized controlled trial

Recruiting
Conditions
asthma
CARA
10006436
Registration Number
NL-OMON46602
Lead Sponsor
eids Universitair Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

maximal 60 patients with asthma in NL (and minimal 30 patients in UK)
* Age 18+
* Clinician diagnosis of asthma
* Asthma treatment step 2-5 - need for regular controller medication (*6 months of the year), this equates to 2 or more ICS prescriptions per year
* Poor asthma control (ACQ>0.75) and/or one-or-more exacerbations or hospital visit in the previous year due to asthma
* Ownership of a mobile phone compatible with the myAirCoach system (Android operating system)

Exclusion Criteria

* Unable to understand Dutch or English, as appropriate

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Primary objective<br /><br>To assess whether self-management support by the myAirCoach system as an<br /><br>adjunct to usual care improves asthma control in patients with asthma, compared<br /><br>to usual care.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondary objectives<br /><br>* To determine whether the myAirCoach system improves quality of life, asthma<br /><br>exacerbations and FeNO and lung function level<br /><br>* To determine whether the myAirCoach system improves adherence to medications<br /><br>and asthma self-management<br /><br>* To determine users* acceptance of the myAirCoach system and identify<br /><br>potential issues to the implementation of the system<br /><br>* To assess cost-effectiveness and organisational impact of the myAirCoach<br /><br>system, compared to usual care<br /><br>* To determine whether the Philips Air Purifier improves asthma control,<br /><br>quality of life and exacerbation rate</p><br>
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