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

Recruiting N/A Interventional Study
Epilepsy Seizure
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
14 – 24
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
200 (estimated)
Sponsor
University of Central Florida · Other
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About This Trial
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 (u…
Trial Locations
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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-in…
Contacts

Michelle Tall, PhD, RN, FAES

4077970555

Michelle.Tall@UCF.edu

CONTACT

Amoy Fraser, PhD, CCRP, PMP

4072668742

Amoy.Fraser@UCF.edu

CONTACT