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Study identifier: NCT05572177 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Feasibility of a Smartphone Application for Asthma Self-management

Condition: Asthma Chronic  ·  Sponsor: University of South Florida

PhaseNA
Planned participants50
Who can joinAll sexes, 12 Years to 17 Years
Healthy volunteersNo

About this study

The primary goal of this project is to determine the feasibility, acceptability, and adherence of a smartphone application for improving asthma self-management in a pilot randomized controlled trial (RCT). The app is specifically designed to appeal to adolescents. Adolescents with persistent asthma will be randomized to receive: 1) standard-of-care or 2) the self-management app in addition to standard-of-care. Feasibility will be assessed by the ability to recruit and retain subjects, technical barriers to implementation, and the appropriateness of the intervention among adolescents and providers. The acceptability of the intervention will be determined by appraising perceived usefulness, entertainment, and ease of use of the app. Adherence to usage of the app over a 6-month period will be assessed by examining the frequency of app usage and the features that were used, and the extent of data regarding self-management that was entered. A secondary objective is to obtain preliminary estimates of effectiveness of the app on clinical outcomes (ACT score, spirometry, CHSA-C, exacerbations, and medication adherence) relative to standard-of-care. It is hypothesized that the app will result in a high level of adherence and will be a feasible and acceptable intervention to improve self-management among adolescents with persistent asthma.

This description comes directly from the study's public registry record.

Talk to the study team

Dipti Karnani  ·  813-974-5193  ·  diptik@usf.edu

Nataliya Kuzmin  ·  813-974-9157  ·  Nataliyak@usf.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of South FloridaTampa, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05572177