Effect of the EpiSchool-M App on Teachers' Epilepsy Knowledge, Attitudes, and Self-Management (EpiSchool-M)

May 5, 2025 updated by: Zahide İYİ ALTINIŞIK, Kafkas University

The Effect of Epilepsy Management at School Mobile Health Application on Epilepsy Knowledge, Attitudes, and Self-Management of Teachers of Children With Intellectual Disability: A Randomized Controlled Study

The aim of this study was to determine the effects of the training given to the teachers of children with intellectual disabilities with the "Epilepsy Management at School Mobile Health Application" and the "Digital Epilepsy Education Guide" on teachers' epilepsy knowledge, attitudes, and self management levels. This study was planned in a pretest, posttest design, follow-up, randomized controlled study. The sample of the study will consist of 90 teachers. Intervention-1 (Epilepsy Management at School Mobile Health Application, n=30), intervention-2 (Digital Epilepsy Education Guide, n=30) and control group (group without any intervention, n=30) will be included in the study. The data collection tools to be used in the research will be applied to all three groups at the same time intervals (T0: Just before the application phase of the research, T1: 15 days after the application, T2: one month after the application). The data will be collected using the Personal Information Form, the Knowledge and Attitudes Toward Epilepsy Among School Teachers Scale, and the Epilepsy Self-Management Scale for Teachers. Statistical Package for the Social Sciences (SPSS) 25.0 package program will be used in the analysis of the data.

Study Overview

Study Type

Interventional

Enrollment (Actual)

90

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Konyaaltı
      • Antalya, Konyaaltı, Turkey, 07070
        • Akdeniz University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Working at special education schools affiliated with the Ministry of National Education in Antalya Province,
  • Teachers of children with moderate to severe intellectual disabilities,
  • Having a smartphone with internet access and either an Android or iOS operating system.

Exclusion Criteria:

  • Teachers of children with hearing and visual impairments, without intellectual disabilities
  • Teachers of children with mild intellectual disabilities

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Mobile Application Group
Teachers in the Epilepsy Management at School Mobile Health Application group will download the EpiSchool app to their phones. Within two weeks, they will watch the epilepsy-related educational videos and the animation video integrated into the app.
Teachers who meet the inclusion criteria will use the EpiSchool
Experimental: Digital Education Guide Group
The digital guide, prepared based on expert opinions, will be sent to the teachers via a link. They will be asked to read the guide within 15 days.
Teachers who meet the inclusion criteria will use the EpiGuide
No Intervention: Control Group
Group without any intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge And Attitudes Toward Epilepsy Among School Teachers Scale
Time Frame: 1.5 months

The scales developed by Kos et al. (2023) assess knowledge and attitudes toward epilepsy. A higher total score indicates a higher level of knowledge and attitude. The scales consist of two parts: the "Attitudes Toward Epilepsy Among School Teachers Scale" and the "Knowledge Toward Epilepsy Among School Teachers Scale." The "Attitudes Toward Epilepsy Among School Teachers Scale" has two subdimensions: attitudes toward social relationships of children with epilepsy (10 items) and attitudes toward epilepsy-related limitations (5 items), totaling 15 items. A lower score on this scale indicates more positive attitudes toward epilepsy.

The "Knowledge Toward Epilepsy Among School Teachers Scale" includes two subdimensions: knowledge about epilepsy (2 items) and knowledge about epilepsy's effects (10 items), totaling 12 items. A lower score on this scale indicates higher knowledge about epilepsy.

Both scales are five-point Likert-type measurement tools.

1.5 months
Epilepsy Self-Management Scale for Teachers
Time Frame: 1.5 months
The Epilepsy Self-Management Scale for Teachers, developed by Kos et al. (2022), aims to assess epilepsy self-management in teachers. It is a 23-item, five-point Likert scale. Responses are numbered from 1 to 5, with 1 meaning "Never" and 5 meaning "Always." Each item on the scale can receive a score between 1 and 5. The scale consists of three subdimensions: the first subdimension is seizure-related self-management (13 items), the second subdimension is pre-seizure self-management (5 items), and the third subdimension is post-seizure self-management (5 items).
1.5 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 10, 2025

Primary Completion (Actual)

March 24, 2025

Study Completion (Actual)

April 24, 2025

Study Registration Dates

First Submitted

January 23, 2025

First Submitted That Met QC Criteria

January 31, 2025

First Posted (Actual)

February 4, 2025

Study Record Updates

Last Update Posted (Actual)

May 8, 2025

Last Update Submitted That Met QC Criteria

May 5, 2025

Last Verified

May 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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