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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

76 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-11-29

Study Completion Date

2025-06-20

Brief Summary

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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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Detailed Description

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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.

Conditions

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Febrile Convulsion

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

The study included two groups: an intervention group and a control group.

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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control

No video-based educational intervention was administered to the control group

Group Type OTHER

The video based education group

Intervention Type 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.

Interventions

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The video based education group

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

Intervention Type OTHER

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes