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AI-Based Mobile Intervention on Medication Non-Adherence and Transition

Recruiting

Who can join

Ages 14 to 24 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Diagnosed with epilepsy
* Currently prescribed anti-seizure medicine (ASMs)
* Identified as part of an underserved population, defined as meeting at least one of the following: member of a racial or ethnic group historically underrepresented in research or healthcare or low-income status (e.g., eligible for public assistance or government-subsidized health coverage)
* Are between 14-17 years old and able to provide assent, with a parent or LAR present to receive app notifications throughout the study
* Are between 18-24 years old and able to provide informed consent
* Able to read, speak, and write in English
* Resides in Florida
* Receive outpatient medical services

Exclusion Criteria:

* They do not own a mobile device with internet access.
* They have a history of severe intellectual disability.
* They are unable to operate a mobile device (keyboard or touchscreen).
* Reside in an in-patient setting.
* Adults unable to consent.
* Pregnant women (excluded because pregnancy is not relevant to the study focus).
* Prisoners.

About the study

This study aims to examine whether the AI-personalized version of the Medilepsy® app is more effective than the non-AI (standard version without AI personalization) can improve key outcomes, such as medical adherence and transition readiness, among underserved adolescents and young adults with epilepsy, ages 14-24, in Florida, USA.

Outcomes are organized into primary (effectiveness), secondary (usability), and exploratory (language experience) endpoints.

What is being tested

Sponsor: University of Central Florida · Participants: 200 · Started: 2026-05

Contact the study team

Official record on ClinicalTrials.gov — NCT07445074

Locations in the U.S.

FloridaOrlando Health Arnold Palmer Hospital, Orlando
Orlando Health Orlando Regional Medical Center, Orlando

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.