Animation Supported COVID-19 Education (COVID-19)

November 29, 2022 updated by: Sidar Gül, Siirt University

The Effect of Animation-Supported Education Based on the Health Promotion Model for Protection From COVID-19 Disease on Primary School Students

Introduction: The COVID-19 epidemic and related mutations, which affect the whole world, continue to increase globally. In particular, this crisis adversely affects school-age children's quality of life.

Method: The study was carried out between February and April 2022 following the experimental research criteria with the pretest-posttest-retest control group. The research population consists of 4th-grade primary school students studying in schools affiliated with the Siirt Directorate of National Education. The sample consists of 148 students studying in the 4th grade at two schools deemed suitable for the conduct of the study. Data were collected using data collection materials, the Descriptive Questionnaire, and the General Child Quality of Life Scale.

Results: The mean age of all students participating in the study was 10.53±2.60, 53% of the students were girls, and 47% were boys. It has been determined that 36.0% of the Students have not received any training on COVID-19 before, 32.4% of them did not take precautions to defend themselves from COVID-19 disease, and it is not possible to protect 48.4% of them from COVID-19 disease even if adequate precautions are taken. It was found that the difference between the pretest, posttest, and retest mean scores of the Students in the experimental group on the quality of life scale was statistically significant (p < 0.05). It was determined that the mean of life quality increased immediately after the training but decreased in the measurements one month later.

Conclusion: Education to be given to school-age children should be developed with animation-supported programs.

Study Overview

Status

Completed

Conditions

Detailed Description

The new type of Coronavirus Disease (COVID-19), which emerged in China in December 2019, has spread rapidly worldwide. It was declared a global pandemic by the World Health Organization on March 11, 2020 (WHO, 2020). COVID-19 poses a significant threat to the entire society. For this, educational institutions that seem to be risky among the measures taken worldwide have been closed (1). For this reason, it has been decided to continue all education activities through distance education from November 20, 2020, until January 4, 2021. Afterward, it was decided to conduct face-to-face education and training activities in certain stages (2,3).

The importance of education and information activities to prevent COVID-19 disease and reduce the spread of the disease is indisputable. Due to the initiation of face-to-face education, informing school-age children about prevention from the epidemic plays a crucial role in making the school environment safe (4). One of the methods that can be used to inform school-age children about COVID-19 is animations created within the scope of play therapy because animations provide psychomotor, cognitive, social, and emotional development of children and give them positive behaviors and habits (5-7). Concordantly, nurses who stay in close and long-term communication with children, as are with all segments of society, have tremendous responsibilities. Providing accessible, accurate, and evidence-based health information about the epidemic is among the accountabilities of nurses (8). Benefiting from theories and models that offer a professional approach to nursing has many benefits, such as increasing the quality of education, guiding practice, and increasing the health level of individuals (9). For this purpose, the health promotion model (10), created by Pender is suitable to be used in nursing studies carried out to protect against COVID-19 disease

Study Type

Interventional

Enrollment (Actual)

148

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Siirt, Turkey, 56100
        • Siirt University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

8 years to 12 years (CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Being at school between the study dates
  • Volunteering of the students' and parents' willingness to participate in the research

Exclusion Criteria:

  • The presence of a communication problem in the participant

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Experimental
An animation-supported training based on the health promotion model for COVID-19 disease and prevention measures was given to the participants.
Expert support was received for the design and preparation of animation videos.
NO_INTERVENTION: Control
No intervention was applied to the participants in the control group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Socio-demographic Questionnaire
Time Frame: Baseline
This form was developed by the researchers in line with the literature and consists of 10 questions. In the form, there are five questions about the students' socio-demographic characteristics and five queries about their knowledge and perceptions of the COVID-19 disease.
Baseline
Generic Quality of Life Instrument for Children (Kid-KINDL)
Time Frame: Baseline
The questionnaire consists of 6 subscales; Physical state, psychological well-being, self-worth, family, friend, and school subscales. The scale consists of 30 items in a 5-point Likert type. High scores indicate a healthy quality of life.
Baseline
Generic Quality of Life Instrument for Children (Kid-KINDL)
Time Frame: At the end of the 1st week
The questionnaire consists of 6 subscales; Physical state, psychological well-being, self-worth, family, friend, and school subscales. The scale consists of 30 items in a 5-point Likert type. High scores indicate a healthy quality of life.
At the end of the 1st week
Generic Quality of Life Instrument for Children (Kid-KINDL)
Time Frame: At the end of the 4th week
The questionnaire consists of 6 subscales; Physical state, psychological well-being, self-worth, family, friend, and school subscales. The scale consists of 30 items in a 5-point Likert type. High scores indicate a healthy quality of life.
At the end of the 4th week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

February 1, 2022

Primary Completion (ACTUAL)

April 30, 2022

Study Completion (ACTUAL)

July 30, 2022

Study Registration Dates

First Submitted

November 29, 2022

First Submitted That Met QC Criteria

November 29, 2022

First Posted (ACTUAL)

December 1, 2022

Study Record Updates

Last Update Posted (ACTUAL)

December 1, 2022

Last Update Submitted That Met QC Criteria

November 29, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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