NCT07027501

Brief Summary

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.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
76

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 29, 2024

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 7, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

May 21, 2025

Completed
28 days until next milestone

First Posted

Study publicly available on registry

June 18, 2025

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 20, 2025

Completed
Last Updated

June 18, 2025

Status Verified

June 1, 2025

Enrollment Period

1 month

First QC Date

May 21, 2025

Last Update Submit

June 16, 2025

Conditions

Keywords

febrile convulsion, fever, education, QR

Outcome Measures

Primary Outcomes (1)

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

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

Study Arms (1)

control

OTHER

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

Other: The video based education group

Interventions

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

control

Eligibility Criteria

Age18 Years+
Sexall(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bulent Ecevit University

Zonguldak, 67300, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Seizures, FebrileFever

Condition Hierarchy (Ancestors)

SeizuresNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsBody Temperature Changes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Model Details: The study included two groups: an intervention group and a control group.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 21, 2025

First Posted

June 18, 2025

Study Start

November 29, 2024

Primary Completion

January 7, 2025

Study Completion

June 20, 2025

Last Updated

June 18, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share

The data collected include sensitive personal and health information, and participants were not explicitly informed or consented to data sharing beyond the scope of this study. Therefore, to protect participant confidentiality and comply with ethical guidelines, the IPD will not be shared with other researchers.

Locations