The Effect of Web-based Education Provided According to the Health Promotion Model on Self - Management in Epilepsy Patients

NCT06194916 | Unknown

• 1 other identifier: AtaturkU-HMŞRLK-SU-01
• Study Type: interventional
• Target: 100
• Locations: 0 countries
• Sites: N/A

Brief Summary

Epilepsy is a disease that requires long-term treatment and follow-up. Epilepsy To be successful in management, the educational needs of the patient must first be determined and the individual Treatment compliance should be increased by ensuring self-management of the disease.Interventions planned based on the model in patient education direct caregivers to specific goals and provide more planned, coordinated and safe care. The Health Promotion Model (HGM), developed by Nola Pender, is one of the models used to explain health protection and promotion behaviors. It is not aimed at preventing any disease or disability, but aims to improve health, in other words, to further increase the general health and well-being of the individual. H0: Web-based education given to epilepsy patients according to the Health Promotion Model has no effect on self-management. H1: Web-based education given to epilepsy patients according to the Health Promotion Model has an effect on self-management. Research Inclusion Criteria:

1. 1.Individuals who agree to participate in the research
2. 2.Being over 18 years of age
3. 3.Having been diagnosed with epilepsy for at least 1 year
4. 4.Being able to use technological devices (phone, computer, tablet)
5. 5.Having internet access,
6. 6.Being able to speak Turkish,
7. 7.Not having any additional disease
8. 8.Being literate When starting the study, patients who apply to the outpatient clinic and meet the inclusion criteria will be given an explanation about the purpose of the research and how the research process will work. Then, written consent will be obtained indicating that they agree to participate in the study. Pretest data will be collected online. "Personal Information Form" and "Epilepsy Self-Management" scale will be used for individuals in the control and experimental groups to collect data.

Conditions

Epilepsy

Keywords

epilesy,education,self management

Outcome Measures

Primary Outcomes (1)

• Personal Information Form Epilepsy Self-Management Scale

  pre-educationup to 4 weeks up to 8 weeks

Secondary Outcomes (1)

• Epilepsy Self-Management Scale

  3 months after the education is completed

Study Arms (2)

education group

EXPERIMENTAL

A 4-week web-based self-management training will be administered to epilepsy patients in the experimental group.

Other: Education

Control Group

ACTIVE COMPARATOR

routine interventions

Other: CONTROL GROUP

Interventions

Education OTHER

A 4-WEEK SELF-MANAGEMENT TRAINING WILL BE PROVIDED THROUGH THE WEB-BASED TRAINING SITE.

education group

CONTROL GROUP OTHER

THEY WILL RECEIVE THE ROUTINE CARE GIVEN TO PATIENTS WITH EPILEPSY.

Control Group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Individuals who agree to participate in the research
• Being over 18 years of age
• Having been diagnosed with epilepsy for at least 1 year
• Being able to use technological devices (phone, computer, tablet)
• Having internet access,
• Being able to speak Turkish,
• Not having a psychiatric disease.

You may not qualify if:

• \. Individuals who do not agree to participate in the research 2. Those under 18 years of age 3. Those with a psychiatric illness 4. Those who cannot use technological devices 5. Those who do not speak Turkish 6. Those diagnosed in less than 1 year

Sponsors & Collaborators

• Ataturk University: lead

MeSH Terms

Conditions

Epilepsy

Interventions

Educational Status; Control Groups

Condition Hierarchy (Ancestors)

Brain Diseases; Central Nervous System Diseases; Nervous System Diseases

Intervention Hierarchy (Ancestors)

Socioeconomic Factors; Population Characteristics; Epidemiologic Research Design; Epidemiologic Methods; Investigative Techniques; Research Design; Methods

Central Study Contacts

şuheda üstündağ

CONTACT

05419281997; ustundagsuheda@gmail.com

nuray bingöl

CONTACT

05054551238; nuraydayapoglu@hotmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, OUTCOMES ASSESSOR
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: science expert

Study Record Dates

• First Submitted: December 22, 2023
• First Posted: January 8, 2024
• Study Start: March 1, 2024
• Primary Completion: June 1, 2024
• Study Completion: September 1, 2024
• Last Updated: January 8, 2024

Record last verified: 2023-12

Data Sharing

• IPD Sharing: Will share
• Shared Documents: STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE