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Recruiting Not applicable

Evaluation of a Digital Tool to Improve Aeroallergen Immunotherapy Adherence. NavigAITme Project

NCT07419230 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-03-11
Last updated
2026-03-23

Condition(s) studied

Allergic Rhinitis

Investigational drug(s) / intervention(s)

Active Adherence-booster AppInactive Adherence-booster App

Active Adherence-booster App: The Active Adherence-booster App includes an array of short messages that will be delivered to the active arm participants to tackle previously reported factors negatively influencing adherence in AIT, such as patient´s knowledge on Allergic rhinitis and AIT as well as administration and purchase reminders. The App will also serve as electronic Case Report Form

Inactive Adherence-booster App: The Inactive Adherence-booster App does not include any of the messages or intervention of the Active version. The App only serves as electronic Case Report Form

Study summary

Aaeroallergen Immunotherapy (AIT) is indicated in the treatment of allergic rhinitis and asthma, and has shown efficacy to control symptoms and induce immunomodulatory changes that support post discontinuation efficacy. Data from clinical trials provides founding for its efficacy and safety profile, but the therapy needs to be withheld for a minimum of 3 years, with modalities that imply daily or near daily administration of a sublingual extract, or subcutaneous injections, every 4 to 6 weeks. This treatment regimen often faces other limitations such as cost, patient´s lack of knowledge regarding efficacy/safety, or potentiality of adverse reactions. These factors have been pointed out as main reasons for a reported low level of treatment adherence in real life.

While overall literature data on treatment adherence ranges widely, from 6% to 93% of patients finalising the minimum of 3 years, current data from precise German registries inform of persistence at 3 years being very low, varying from 5.2% to 18.2% with differences depending on extract, route and patient´s age.

Surprisingly, even if the Scientific community acknowledges patient adherence as a very relevant weak point, there´s paucity of structured strategies to tackle this issue, and those available, have mostly been developed in single centers, for periods below the 3 years of AIT recommended duration. In the era of technology, and with the spreading of mobile applications (App), new approaches are currently ongoing to counteract this important drawback . In this landscape, this study aims at creating a new App that will be thoroughly tested in a prospective long-term randomized trial, to improve AIT persistence.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients of any age and sex * Patients who have received their first prescription for a new aeroallergen immunotherapy treatment as part of their routine care for allergic rhinitis with or without asthma * Patients who have been prescribed only a single immunotherapy product * Patients who have been prescribed a commercially available product, from any company, for sublingual or subcutaneous administration * Patients who have provided the first photograph of the product for which they are entering the study Exclusion Criteria: * Patients receiving AIT prescription for asthma only, and do not suffer allergic rhinitis * Administration routes other than subcutaneous or sublingual * Patients receiving AIT prescription for other indications, e.g., food or hymenoptera allergies * Patients who have received immunotherapy in the last 3 years or are currently undergoing treatment with an AIT product other than the one being studied in the current project. * Patients who have received prescription for two or more different immunotherapy products simultaneously

Primary outcome measure(s)

  • Comparing the proportion of subjects who maintain therapeutic persistence after completing 3 years of Immunotherapy treatment in the active and control groups — From entry to the end of study period at 3 years
    Persistence definition: time from the moment of delivery of the first product, until the estimated time of completion of the last product delivered. This definition has been previously used in this field. A difference of 15% between active and control groups will be considered as clinically meaningful, denoting success of the intervention

Trial sites (1)

FacilityCityRegionStatus
Hospital Infantil Universitario Niño Jesús. Avenida de Menéndez Pelayo, número 65 Madrid Madrid Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07419230 on ClinicalTrials.gov ↗ ← All trials in Spain