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RECRUITING
NCT07445074
NA

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

Sponsor: University of Central Florida

View on ClinicalTrials.gov

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.

Key Details

Gender

All

Age Range

14 Years - 24 Years

Study Type

INTERVENTIONAL

Enrollment

200

Start Date

2026-03

Completion Date

2026-12

Last Updated

2026-03-03

Healthy Volunteers

No

Conditions

Interventions

OTHER

Medilepsy® Chatbot AI-Enhanced

Participants 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.

OTHER

Medilepsy® Chatbot Standard

Participants 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.

Locations (1)

University of Central Florida

Orlando, Florida, United States