Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

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

NCT07445074 · View on ClinicalTrials.gov ↗

Study 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 Studied

Interventions

  • OTHER Medilepsy® Chatbot AI-Enhanced
  • OTHER Medilepsy® Chatbot Standard

Study Locations (1)

Florida

  • University of Central Florida — Orlando

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2026-03
Est. Completion 2026-12
Phase NA

Sponsor

University of Central Florida

189 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07445074

The ClinicalTrials.gov registry entry for NCT07445074 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Central Florida, which has 189 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Epilepsy appearing as the primary indexed condition, and to 2 interventions — of which Medilepsy® Chatbot AI-Enhanced is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07445074 reports 1 study location spanning 1 distinct geographic area — top geographies include Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07445074 about?

NCT07445074 is a clinical study titled "AI-Based Mobile Intervention on Medication Non-Adherence and Transition". 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 epile...

What is the current status of trial NCT07445074?

This trial is currently recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2026-03. Estimated completion is 2026-12.

What conditions does trial NCT07445074 study?

This clinical trial studies the following conditions: Epilepsy, Seizure. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07445074?

The interventions under investigation include: Medilepsy® Chatbot AI-Enhanced (OTHER), Medilepsy® Chatbot Standard (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07445074?

This trial is sponsored by University of Central Florida, which has 189 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07445074 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial