About this trial
The primary objective consists in the comparison of the combined symptom medication score values between (i) patients randomised to the early warning system personalised forecasting messages, and (ii) patients randomised to generic messages already delivered by MASK-air®.
The combined symptom medication score has recently been developed in a data-driven way and validated (https://eaaci.org/images/CSMS.pdf); it assesses allergic rhinitis control taking into account both reported symptoms and medication use.
As secondary objectives, visual analogue scales on allergic rhinitis symptoms (VAS global, nasal, eye, asthma), and medication use will also be separately compared.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
Illiterate patients
Patients without smartphone
Patients who are not able to complete a daily monitoring questionnaire on allergic rhinitis.
Trial design
Parallel
Treatments tested in this trial
Personalised early warning system
Combination productEarly warning system personalised forecasting messages
Treatment groups
Trial outcomes
Primary outcomes
Combined symptom medication score values
Daily symptom and medication data provided by patients allow the calculation of two validated daily combined symptom-medication scores from formulae previously published: * the CSMS (combined symptom-medication score) * e-DASTHMA.
Sponsors and contacts
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Universidade do Porto
Lead sponsor
Centro Hospitalar De São João, E.P.E.
Collaborator
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