New app aims to boost cystic fibrosis treatment adherence
NCT ID NCT07031323
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study is testing a smartphone app called OnTrackCF, designed to help adults with cystic fibrosis remember to take their CFTR modulator medication and track their symptoms. The app sends up to 3 daily support messages and shows users their adherence levels. Researchers want to see if the app is easy to use, acceptable, and engaging for 60 adults with CF. The study does not test a new drug, but a behavioral tool to support existing treatment.
What this could mean
Our plain-language read of the trial. This is informational only โ not medical advice or a prediction.
- Active substance
- OnTrackCF smartphone app (behavioral intervention)
- What this could lead to
- If successful, this app could help people with cystic fibrosis better manage their daily medication and symptoms, improving adherence and quality of life.
- What could go wrong
- This is a small, early feasibility study with only 60 participants, so results may not apply to everyone. The app's benefits depend on user engagement and may not lead to long-term health improvements.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Boston Children's Hospital
RECRUITINGBoston, Massachusetts, 02115, United States
-
Johns Hopkins University
NOT_YET_RECRUITINGBaltimore, Maryland, 21218, United States
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University of Alabama-Birmingham
NOT_YET_RECRUITINGBirmingham, Alabama, 35233, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Could modern CF drugs make daily inhaled treatments obsolete?
- New study investigates hidden heart risks in cystic fibrosis patients on modern drugs
- Blood pressure drug may help preserve insulin in cystic fibrosis
- Hidden toll: depression and anxiety in kids with cystic fibrosis
- Air pollution may worsen cystic fibrosis in kids, study hopes to find out