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NCT Number: NCT07027501

The Evaluation of the Effectiveness of Febrile Seizure Training Given to Parents

Objective: The aim of this study was to evaluate the effectiveness of a video-based educational intervention delivered via QR code to parents of hospitalized children aged 6 months to 5 years-an age group in which febrile seizures are most commonly observed.

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This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Bulent Ecevit University

Zonguldak, 67300, Turkey (Türkiye)

About this study

Method: This study will be designed as a randomized controlled trial. The study population will consist of parents of children aged between 6 months and 5 years who are hospitalized in the pediatric wards of Kdz. Eregli State Hospital during the data collection period (September 1, 2024 - September 1, 2025). The sample will include 100 parents-50 in the intervention group and 50 in the control group-who meet the inclusion criteria.

Eligibility criteria for sampling; The child must have been hospitalized. The child must be between 6 months and 5 years of age. The parent must be able to speak and understand Turkish. The parent must agree to participate in the study Data collection: Between September 1, 2024, and September 1, 2025, the "Child and Parent Introductory Information Form" and the "Febrile Convulsion Knowledge Level Scale for Parents/Caregivers" will be completed by participants who meet the eligibility criteria.

No educational session or brochure will be provided to the control group. In the intervention group, after completing the "Child and Parent Introductory Information Form " and the "Febrile Convulsion Knowledge Level Scale for Parents/Caregivers", participants will be shown the educational brochure and granted access to the video training via the QR code included in the brochure.

At the end of the training, the "Febrile Convulsion Knowledge Level Scale for Parents/Caregivers" will be administered again. The brochure used in the training will be distributed to all participants in the intervention group.

Four weeks after the training, participants in the intervention group will be contacted again, and their data will be recollected using the same scale to assess knowledge retention and the long-term effectiveness of the training. Similarly, in the control group, the "Febrile Convulsion Knowledge Level Scale for Parents/Caregivers "will be re-administered four weeks after the initial data collection.

Data Analysis:

The data will be analyzed using the SPSS version 27.0 software.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

The child has been hospitalized. The child is between 6 months and 5 years old. The parent can speak and understand Turkish. The parent agrees to participate in the study.

Exclusion criteria

The child has not been hospitalized. The child is younger than 6 months. The child is older than 5 years. The parent or legal guardian cannot speak or understand Turkish. The parent does not agree to participate in the study.

Treatment and study plan

The video based education group

Other

The parents in the intervention group were provided with a video-based educational material on febrile seizures, which they accessed via a QR code.

Primary outcomes

  1. Outcome Measure Title: Change in Knowledge Levels Regarding Febrile Seizures Among Parents, Measured by the Febrile Seizure Knowledge Assessment Questionnaire

    Time frame: Knowledge scores were measured at baseline, immediately after training (1 hour later), and 4 weeks later in both intervention and control groups.

Sponsors and collaborators

Lead sponsor

Zonguldak Bulent Ecevit University

Other

Registry information

Official study title

The Evaluation of the Effectiveness of Febrile Seizure Training Given to Parents of Children Aged 6 Months to 5 Years

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jun 18, 2025
Registry last updated
Jun 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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