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Epilepsy Enhanced Care

Evaluating the Impact of Epilepsy Enhanced Care on Health Literacy in People With Epilepsy: A Nurse-led Educational Intervention Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07709481
Enrollment
166
Registered
2026-07-16
Start date
2026-08-01
Completion date
2028-08-01
Last updated
2026-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epilepsy

Brief summary

Background: Epilepsy is a common brain condition that causes repeated seizures. People with epilepsy often need a lot of information to manage their health, but many do not receive enough education about their condition. Having good health literacy (the ability to find, understand, and use health information) is important for managing epilepsy well. Objective: This study aims to test whether a special educational program led by a trained epilepsy nurse, called "Epilepsy Enhanced Care," helps adults with epilepsy better understand and manage their health. Study design: This is a prospective, non-randomized, controlled study involving adults (aged 18 years or older) with epilepsy. Participants will be divided into three groups: * Intervention group: Patients with newly diagnosed epilepsy who will receive the "Epilepsy Enhanced Care" educational program in addition to their usual care. * Control group 1: Patients with newly diagnosed epilepsy who will receive only their usual care. * Control group 2: Patients who have had epilepsy for at least one year and will receive only their usual care. Intervention: The "Epilepsy Enhanced Care" program is a structured, one-on-one educational session delivered by a specialized epilepsy nurse within 2 months of diagnosis. The session covers topics such as epilepsy types, medications, safety planning, and lifestyle management. Patients and their caregivers may attend together. After the session, participants can contact the nurse by phone or email with further questions. Outcomes: The main outcome is the change in health literacy from the start of the study to 3 months after the intervention. Secondary outcomes include changes in epilepsy-specific knowledge, self-management skills, quality of life, anxiety, depression symptoms, and how often patients use healthcare services. Study duration: Participants in the intervention group and control group 1 will be followed for 12 months. Participants in control group 2 will be assessed at a single time point. The entire study is expected to take 24 months. Risks and benefits: The intervention involves only education and counseling, with no medications or medical devices. The risks are minimal, and participation is voluntary.

Interventions

OTHEREpilepsy Enhanced Care

A structured, nurse-led educational program delivered by a specialized epilepsy nurse. Includes a comprehensive consultation (within 2 months after diagnosis) covering epilepsy types, anti-seizure medications, safety planning, lifestyle management. Caregivers encouraged to attend. Follow-up access via telephone/email.

Sponsors

Ente Ospedaliero Cantonale, Bellinzona
Lead SponsorOTHER
Pamela Agazzi
CollaboratorUNKNOWN

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥18 years; * Confirmed epilepsy diagnosis (ILAE criteria); * Ability to provide informed consent (or legal representative); * Sufficient Italian proficiency.

Exclusion criteria

* Previous participation in a structured epilepsy education program; * Severe untreated comorbidities precluding attendance.

Design outcomes

Primary

MeasureTime frameDescription
Improvement in health literacyFrom baseline to 3 months after enrollmentMeasured using Domain 2 ("Having sufficient information to manage my health") of the Health Literacy Questionnaire (HLQ).

Secondary

MeasureTime frameDescription
Changes in scores on other seven domains of the HLQFrom baseline to 3 and 12 months after enrollmentFor each endpoint, the change in score from baseline to follow-up will be measured in the intervention groups, and scores will be compared between the intervention and control groups at follow-up
Change in Epilepsy-specific knowledge scoreFrom baseline to 3 and 12 months after enrollment
Change in Epilepsy Self-Management scoreFrom baseline to 3 and 12 months after enrollment
Change in Generalized Anxiety Disorder 7 scoreFrom baseline to 3 and 12 months after enrollment
Change in Neurological Disorders Depression Inventory for Epilepsy scoreFrom baseline to 3 and 12 months after enrollment
Healthcare utilizationFrom baseline to 3 and 12 months after enrollmentFrequency of epilepsy-related emergency department visits, epilepsy-related hospitalizations, and unscheduled neurology consultations, collected through patient self-report and, where available, verified through electronic medical records.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026