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NCT07663240Enrolling by invitation

Epilepsy Emergency Department High Utilizer Program

Source: ClinicalTrials.gov · Last updated 23 Jun 2026

Brief summary (registry, in English)

We believe that there are many reasons that people with epilepsy get their health care through the emergency department (ED) instead of through primary care or neurology. Our goal is to create program that will address these reasons. The creation of this program will be informed by use of the Grady electronic health records (EHR). We will use the EHR to describe people with epilepsy coming the Grady ED at a high frequency. We create a profile of these patients by examining their demographics and social determinants of health information in their EHR (Aim 1). We will then use that information to create a culturally and medically appropriate program for people with epilepsy (Aim 2). Next, we will test the new program, the Epilepsy Emergency Department High Utilizer Program (Aim 3). We believe this program may improve three things. It will first improve access to care by epilepsy and mental health doctors, and reduce ED visits. It may also help people to manage their triggers, track seizures, and take their medicines on time. And last, we believe it may improve seizure frequency and quality of life for people that are underserved in health care. With the lessons learned from the new program, we will explore ways to sustain the program at Grady and expand it to other health care facilities (Aim 4).

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
15 (estimated)
First submitted
17 Jun 2026
Start date
May 2026
Primary completion date
Dec 2026
Lead sponsor
Morehouse School of Medicine
Diseases
Epilepsy
NCT number
NCT07663240

What you commit to

  • Study type: Observational
  • Planned participants: 15
  • From May 2026 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Regularly taking anti-epileptic medications with established adherence

Other illness

  • No confirmed epilepsy diagnosis (e.g., non-epileptic seizures)
  • Not identified as a high ED utilizer for seizure-related care
  • Unable to provide informed consent due to cognitive impairment or psychiatric instability
  • Complex medical conditions that would limit participation in outpatient follow-up

Age

  • Younger than 18 years of age

Other

  • Scheduled neurology follow-up within 14 days of discharge or consistent primary care follow-up
  • Non-English speaking
  • Pregnant

Who the study is looking for

  • Adult women aged 18 years or older
  • Confirmed diagnosis of epilepsy documented in the electronic health record (EHR)
  • Enrolled in the Grady Health System Transition of Care (TOC) ED High Utilizer Program
  • History of three or more seizure-related emergency department visits within the past 12 months
  • Self-identify as Black or Hispanic
  • Reside in the Atlanta metropolitan area with intent to remain for at least 12 months
  • Have access to a working phone for follow-up communication

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Morehouse School of Medicine
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.