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Effect of a Mobile App on Improving Asthma Control in Patients With Persistent Asthma

Effect of a Mobile App on Improving Asthma Control in Adolescents and Adults With Persistent Asthma: A Pilot Randomized Multicentre, Superiority Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05129527
Acronym
mINSPIRERS_RCT
Enrollment
124
Registered
2021-11-22
Start date
2024-01-31
Completion date
2024-12-31
Last updated
2023-10-19

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

Conditions

Asthma

Keywords

mHealth, smartphone, medication adherence, self-management, technology assessment

Brief summary

mINSPIRERS\_RCT aims to assess the magnitude of the effect of a mobile app for improving asthma control in adolescents and adults with persistent asthma, followed at primary and secondary care in Portugal.

Detailed description

INSPIRERS\_RCT is a pilot randomized, multicenter superiority clinical trial regarding the effect of a mobile app together with usual care (experimental group) in comparison to usual care alone (control group) in adolescents and adults with persistent asthma. The study includes two face-to-face visits (initial visit and at 3 months), and 3 telephone interviews (1 week, 1 month and 4 months), implemented in 32 primary (General Practice) and secondary care centers (Allergy, Pediatrics, Pulmonology) in Portugal.

Interventions

DEVICEInspirerMundi app

Patients in the experimental group, in addition to usual care, will be invited to use the InspirerMundi app for 4 months to support adherence to preventive inhaled medication and their asthma self-management. The purpose of the InspirerMundi app is to transform the adherence process into a positive experience through immediate and pleasant rewards. The InspirerMundi app integrates 3 main components: monitoring (symptoms, control, adherence), gaming and social/peer support. Participants will be able to include their action plan in the app. Within the action plan, the application can lead to changes in the medication effectively taken, which means that the therapeutic level can be adjusted according to the action plan. Participants in the experimental arm will be able to share with their physician, through the app, their medication adherence and asthma control data in the 3 months visit, and whenever patients wish during the study period.

OTHERUsual care

Usual care will consist of pharmacological treatment and medical monitoring through routine medical visits.

Sponsors

Centro de Investigação em Tecnologias e Serviços de Saúde
CollaboratorOTHER
Rede de Investigação em Saúde
CollaboratorOTHER
Universidade do Porto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Age between 13 and 17 years (adolescents) or and between 18 and 64 years (adults); * Previous medical diagnosis of persistent asthma; * Uncontrolled or partially controlled asthma according to Global Initiative for Asthma (GINA) criteria; * Active prescription of inhaled control medication for asthma (all treatments will be accepted. There will be no change in the prescribed therapeutic regimen directly or indirectly related to participation in this study); * Ability to use mobile app and a access (availability and use) to Android mobile devices with internet access; * Do not currently use any mobile application for asthma management.

Exclusion criteria

* Patients diagnosed with chronic respiratory disease other than asthma or, diagnosed with another significant chronic disease, with possible interference with the objectives and/or evaluations of the study. * Patients that participated in previous feasibility studies with InspirerMundi app will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Asthma control (CARAT)Baseline, 3 monthsChange from baseline in the proportion of patients with controlled asthma as assessed with the CARAT-Control of Allergic Rhinitis and Asthma Test at 3 months

Secondary

MeasureTime frameDescription
Change in Number of asthma exacerbations in last 3 monthsBaseline, 3 monthsWorsening asthma events requiring unscheduled health care use (emergency department visit, hospitalization, and/or any medical assistance) or initiation/increase in systemic corticosteroids.
Change in Absenteeism in the last 3 monthsBaseline, 3 monthsNumber of days absent from the workplace/school
Change in Treatment adherence (Test of the Adherence to Inhalers)Baseline, 3 monthsAssessed with Test of the Adherence to Inhalers
Asthma control (GINA)Baseline, 3 monthsChange in Asthma control assessed by the physician acording to GINA (Global initiative for asthma) guidelines
Change in Satisfaction with inhaler1 week, 4 monthsAssessed through 4 visual analogue scales (VAS 0-100, higher number, higher satisfaction)
Change in EuroQol-5 Dimensions (EQ-5D)Baseline, 3 monthsAssessed with EuroQol-5 Dimensions (EQ-5D). Health state index scores generally range from less than 0 (where 0 is the value of a health state equivalent to dead) to 1 (the value of full health), with higher scores indicating higher health utility.
Change in Beliefs about MedicinesBaseline, 3 monthsAssessed with specific Beliefs about Medicines Questionnaire

Countries

Portugal

Contacts

Primary ContactJoão Almeida Fonseca, PhD
jfonseca@med.up.pt(+351) 229027242
Backup ContactCristina Jácome, PhD
cjacome@med.up.pt(+351) 225513622

Outcome results

None listed

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