The Effect of Diabetes Education Given With Video Animation on Metabolic Control, Self-Care Ability, and Attitudes Towards the Disease in Children With Type 1 Diabetes

NCT ID: NCT07107789

Last Updated: 2025-08-06

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

ENROLLING_BY_INVITATION

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-08-15

Study Completion Date

2025-10-06

Brief Summary

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The aim of this study is to evaluate the attitude towards the disease, perceived social support systems, metabolic control and self-care ability of pediatric patients diagnosed with Type 1 diabetes, by giving video animation training considering their age and developmental level. The main questions it aims to answer are:

1. Nursing interventions using video animations increase self-care abilities in children aged 11-18.
2. Nursing interventions using video animations increase the perception of social support in children aged 11-18.
3. Nursing interventions using video animations support metabolic control in children aged 11-18.
4. Nursing interventions using video animations positively affect the attitudes of children aged 11-18 toward their illness.

Detailed Description

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With the development and proliferation of technology, an essential part of our daily lives, adaptation and developments in technology have begun to increase in the healthcare sector. Research has shown that games and video animations are effective methods beyond medication. No studies have been found in the literature evaluating the effects of diabetes education provided through video animation on the metabolic control, self-care abilities, and attitudes toward the disease in children with Type 1 diabetes. Therefore, the aim of this study is to evaluate the effects of video animation education given to children diagnosed with Type 1 diabetes on their attitudes toward the disease, perception of social support, and self-care abilities. It is anticipated that this research will provide a proactive, multifaceted approach to care and treatment. The study was designed as a pretest/posttest randomized controlled trial. The study population consisted of children aged 11-18 who were regularly followed in the outpatient clinic and had been diagnosed with Type 1 diabetes for at least 6 months. Children who accepted the study and met the criteria were assigned to the video animation and control groups using a block randomization method. The study sample was determined to be 80 individuals, 40 in the experimental group and 40 in the control group. The video animation scenario to be used in the study was created by the researchers in parallel with the routine diabetes education provided at the hospital, and expert approval was obtained. The video animation scenes were prepared by a voice actor and illustrator as part of the project. The experimental group will receive diabetes education through video animation following the routine diabetes education provided by the hospital. Pre- and post-intervention surveys will be administered. The control group will receive routine diabetes education from the hospital's diabetes nurse. No other intervention will be administered. Pre-tests/post-tests and surveys will be administered before and after the diabetes education.

Conditions

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Type 1 Diabetes in Children

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two groups, the traditional experimental and control groups
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors
The control group will receive routine diabetes education from the hospital's diabetes nurse. The experimental group will receive diabetes education using a video animation prepared by the researcher following the routine diabetes education provided by the diabetes nurse. The outcome assessment and group allocation will be conducted by a researcher who is unaware of the outcome.

Study Groups

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The experimental group will receive diabetes education through video animation.

Following the routine diabetes education provided by the hospital, the experimental group will receive diabetes education using a video animation prepared by the researcher and approved by an expert. Pre- and post-intervention surveys will be administered.

Group Type ACTIVE_COMPARATOR

Diabetes education with video animation

Intervention Type OTHER

Providing diabetes education to the experimental group through a video animation Following the routine diabetes education provided by the hospital, the experimental group will receive diabetes education using a video animation prepared and staged by the researcher and approved by experts.

Control group to receive routine diabetes education

The control group will receive routine diabetes education from the hospital's diabetes nurse. No intervention will be applied. Only the scale and pre-test/post-test will be administered to the control groups.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Diabetes education with video animation

Providing diabetes education to the experimental group through a video animation Following the routine diabetes education provided by the hospital, the experimental group will receive diabetes education using a video animation prepared and staged by the researcher and approved by experts.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Agreeing to participate in the study
* Diagnosed with Type 1 DM by a specialist
* Diagnosed with Type 1 diabetes for at least 6 months
* Being between the ages of 11 and 18
* Using an insulin pen
* Not using an insulin pump
* Coming for regular checkups at the Pediatric Endocrinology clinic
* Having no other chronic disease besides diabetes

Exclusion Criteria

* Using an insulin pump
* Not being mentally healthy
* Having any mental or physical disability
Minimum Eligible Age

11 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ataturk University

OTHER

Sponsor Role lead

Responsible Party

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Gamze Nur Yılmaz

Phd Student

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Gamze Nur YILMAZ, PhD

Role: PRINCIPAL_INVESTIGATOR

Ataturk University

Locations

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Erzurum City Hospital

Erzurum, Palandöken, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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AU-SBE-GNY-01

Identifier Type: -

Identifier Source: org_study_id

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