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Study identifier: NCT07445074 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Epilepsy · Seizure  ·  Sponsor: University of Central Florida

PhaseNA
Planned participants200
Who can joinAll sexes, 14 Years to 24 Years
Healthy volunteersNo

About this 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.

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

Talk to the study team

Michelle Tall, PhD, RN, FAES  ·  4077970555  ·  Michelle.Tall@UCF.edu

Amoy Fraser, PhD, CCRP, PMP  ·  4072668742  ·  Amoy.Fraser@UCF.edu

Always discuss trial participation with your own doctor first.

Locations (2)

Orlando Health Arnold Palmer HospitalOrlando, Florida, United StatesRecruiting
Orlando Health Orlando Regional Medical CenterOrlando, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07445074