Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07445074

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

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
University of Central Florida · Academic / Other
Sex
All
Age
14 Years – 24 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
OTHERMedilepsy® Chatbot AI-EnhancedParticipants in the intervention group will use the AI-personalized version of the Medilepsy® app, which includes a Smart Chatbot that delivers interactive support based on user-entered data. The chatbot offers personalized prompts, relevant topic suggestions, and adaptive educational content to support epilepsy self-management.
OTHERMedilepsy® Chatbot StandardParticipants in the non-intervention group will use a standard version of the Medilepsy® app without AI functionality. This version includes static prompts and general educational links but does not provide personalized feedback or adaptive interaction.

Timeline

Start date
2026-03-01
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2026-03-03
Last updated
2026-03-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07445074. Inclusion in this directory is not an endorsement.