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CompletedNCT04144478Updated Nov 1, 2019

Web-Based Epilepsy Education Program for Adolescents and Parents

An interventional study of Web based education in Epilepsy, sponsored by Suleyman Demirel University. Completed at 1 site in Turkey. Open to participants aged 12 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-11-01.

Sponsored by Suleyman Demirel University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 1 year 11 months after the study started (first participant enrolled Nov 2017, registered Oct 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
140
Allocation
Randomized
Ages
12 Years to 50 Years
Sex
All
01

Study summary

This study aims to develop a web-based epilepsy education program for adolescents with epilepsy and their parents and to evaluate the efficacy of eb-based epilepsy education program on health management.eb-based epilepsy education program has been proved to be a useful and reliable educational website for the development of knowledge, attitude, self-efficacy and e-health literacy of adolescents with epilepsy and their parents.

Read the detailed description

This study aims to develop a web-based epilepsy education program for adolescents with epilepsy and their parents and to evaluate the efficacy of web-based epilepsy education program on health management.

This randomized controlled study was conducted with 69 adolescents with epilepsy aged between 9-18 and their parents (n=71) who were accepted to Pediatric Neurology Policlinic of Antalya Training and Research Hospital of Health Science University between November 2017 and April 2018. The study sample was divided into two groups as study (35 adolescents, 37 parents) and control (34 adolescents, 34 parents) groups using simple randomization method. The web-based epilepsy training program which was developed during the preparation stage of the study was evaluated by 13 experts using the Quality of Criteria for Consumer Health Information measurement instrument. The data collection materials (Seizure Self efficacy scale, E-Health literacy scale, Child Attitude Toward Illness Scale, Website Analysis and MeasureMent Inventory Scale) were administered by the researcher to the adolescents and parents in both groups before applying eb-based epilepsy education program. Following the administration of eb-based epilepsy education program to the initiative group, all participants were observed for three months. The data collection materials were reapplied to all the participants at the end of the third month. In addition, the adolescents and their parents in the study group were applied Website Analysis and Measurement Inventory measurement tool for the evaluation of usability of the site.

02

Conditions studied

  • Epilepsy

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Keywords

  • Epilepsy
  • Web based education
  • Pediatric Nursing
  • Parent
  • Adolescence
03

In context

Epilepsy

1,805 studies on the registry are indexed under Epilepsy; 417 are open to participants now.

This study's enrollment of 140 is above the median of 50 across 1,206 interventional studies indexed under Epilepsy.

Browse Epilepsy studies →

Lead sponsor

Suleyman Demirel University is the lead sponsor of 123 studies on the registry; 36 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Adolescents without mental disability,
  • Followed-up for at least six months with epilepsy diagnosis,
  • No chronic disease other than epilepsy,
  • No photosensitive epilepsy diagnosis,
  • Internet access and use, and parents of these adolescents with internet access and use - were included in the study.

Exclusion criteria

Exclusion Criteria:

  • Adolescents and parents who do not use the Internet
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
140 participants (actual)

Study arms

  • Experimental
    experimental

    Web based education intervention

    Other: Web based education

  • No intervention
    No intervention

    Normal polyclinics application

Interventions

  • OtherWeb based education

    Web based education

06

What researchers measure

Primary outcomes

  1. Epilepsy Knowledge Test

    Epilepsy Knowledge test had applied pre-test and post-test. It consists of true (1), false (0) and I do not know (0) options. The minimum score to be taken from the scale is 0 and the maximum score is 25. The minimum score to be taken from the scale is 0 and the maximum score is 25. The increase in the total score indicates that the level of knowledge has increased.

    Time frame: 12 week

  2. Seizure Self Efficacy Scale

    Seizure Self Efficacy Scale had applied pre-test and post-test. The scale is a 5-point likert with 15 items. It has been interpreterd that the higher the total score, the higher is the self-efficacy level of the individual. The minimum score to be taken from the scale is 15 and the maximum score is 75.

    Time frame: 12 week

  3. Child Attitude Toward Ilness Scale

    Child Attitude Toward Ilness Scale had applied pre-test and post-test. The scale was a 5-point Likert type with 15 items. The minimum score to be taken from the scale is 15 and the maximum score is 75. 25. The minimum score to be taken from the scale is 0 and the maximum score is 25. The increase in the total score indicates that the child has positive attitude own illness.

    Time frame: 12 week

  4. e-Health Literacy Scale

    e-Health Literacy Scale had applied pre-test and post-test. The lowest score that can be obtained from the 5-point Likert scale is 8 and the highest score is 40. A high score from the scale indicates a high level of e-health literacy.

    Time frame: 12 week

  5. Website Analysis and MeasureMent Inventory

    Website Analysis and MeasureMent Inventory had applied both website under preparation and post test for control group.There are 5 dimensions that measure concepts like Attractiveness, Controllability, Efficiency, Helpfulness and Learnability. The total usability score is the weighted combination of expressions from each of the five sub-dimensions. The higher the scores obtained from the scale, the higher is the usability of the website and the more useful it is. The score obtained from the Website Analysis and MeasureMent Inventory is calculated in percentiles. the fact that each sub-dimension is above 50% means that its availability is high.

    Time frame: 12 week

  6. Quality of Criteria for Consumer Health Information

    Quality of Criteria for Consumer Health Information scale is to be used in the assessment of the content and quality of educational material. Quality of Criteria for Consumer Health Information consists of 15 key questions plus an overall quality rating. The low total score indicates a poor quality and the high score indicates a good quality. The minimum score to be taken from the scale is 15 and the maximum score is 75.

    Time frame: 12 week

07

Study locations

1 site
  • Süleyman Demirel University
    Isparta, 32200, Turkey
08

References and documents

Individual participant data

Plan to share: Yes — Research article

Supporting information: Csr

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 1, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04144478
Lead sponsor
Suleyman Demirel University
Responsible party
Şerife TUTAR GÜVEN (Pediatric Nursing, Suleyman Demirel University) — Principal investigator
First posted
Oct 30, 2019
Start date
Nov 1, 2017
Primary completion
Apr 1, 2018
Completion
Jun 28, 2018
Last update
Nov 1, 2019

Study contacts

Ayşegül İşler Dalgıç, Professor
study director · Akdeniz University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2019. You cannot join it, but the record below documents what was studied.

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