- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05632471
The Effect of Web-based Education Given to Parents on Children's Internet Gaming Disorder
March 23, 2023 updated by: Meryem MUTLU, Mersin University
The Effect of Web-Based Education Given to Parents on Children's İnternet Gaming Disorder
Internet Gaming Disorder (IOB) is an important problem that is increasingly prevalent all over the world and can be prevented before it develops.
This research is a single-blind, randomized controlled experimental study to evaluate the effect of Internet-based education given to parents on children's Internet gaming disorder.
96 children and their parents studying in the central districts of a province and at risk for the development of IOBB were divided into intervention (48) and control groups (48) according to the randomization list.
The "I know digital games" training consisting of three modules and 10 videos was given to the intervention group via the website prepared by the researchers, and no intervention was made to the control group.
The research data were collected at three different times using the "Internet Gaming Disorder Scale Short Form" (İOOBÖ9-SF) and the forms developed by the researchers.
In the analysis of data; descriptive statistics, Chi-square, Mann Whitney U test, and repeated measures ANOVA were used.
Before the analysis, eight missing data in the control group were estimated with regression estimation models from intent to treat protocols.
Statistical significance level p ≤0.05 was taken in all analyzes.
Parents and children in the intervention and control groups were similar in terms of sociodemographic characteristics and playing characteristics (p>0.05).
It would be beneficial to involve parents in the interventions that nurses will make for primary school children in order to prevent IOB.
Study Overview
Status
Recruiting
Conditions
Study Type
Interventional
Enrollment (Anticipated)
96
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 Contact
- Name: Meryem Mutlu Sayın
- Phone Number: 05330949169
- Email: meriyemmutlu@gmail.com
Study Contact Backup
- Name: Sümbüle Köksoy Vayısoğlu
- Phone Number: 05075050711
- Email: sumbule@mersin.edu.tr
Study Locations
-
-
Antakya
-
Hatay, Antakya, Turkey, 31100
- Recruiting
- Meryem MUTLU SAYIN
-
Contact:
- Sümbüle SÜMBÜLE KÖKSOY VAYISOĞLU
-
-
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
9 years to 10 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
For kids
- To have a score between 25-36 from IOOBÖ9-SF [69]
- Willingness to participate in the study,
- No communication barrier,
- Being educated in high socioeconomic level schools,
- Not having a psychiatric diagnosis and/or not using psychiatric medication
for parents
- Your child's score between 25-36 on IOOBÖ9-SF,
- Willingness to participate in the study,
- No communication barrier,
- Having at least one tablet/smartphone/computer and being able to use these devices,
- Having mobile or home internet,
- Being literate,
- The parent who will participate in the study does not have a psychiatric diagnosis and/or uses psychiatric medication.
Exclusion Criteria:
For kids
- Having received 25 points below or 36 points above IOOBÖ9-SF
- Not being willing to participate in the study,
- Having a communication barrier (not being able to speak or understand Turkish…),
- Having a psychiatric diagnosis and/or using psychiatric medication
for parents
- Your child's score below 25 or above 36 on OOOBÖ9-SF
- Not being willing to participate in the study,
- Having a communication barrier (not being able to speak or understand Turkish…)
- Not having at least one tablet/smartphone/computer,
- Not having mobile or home internet,
- Being illiterate,
- The parent who will participate in the study does not have a psychiatric diagnosis and/or uses psychiatric medication.
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 Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: web-based training for parents in the intervention group
Parents were given "I know digital games" training with 10 videos from the website.
|
"I know digital games" training consisting of 10 web-based videos
|
|
Other: parents in the control group
No intervention was applied to the parents in the control group.
|
The control group was not trained
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Internet Gaming Disorder Scale Short Form (IGDS9-SF) score
Time Frame: 4 months
|
An increase in the scale scores means that the problematic behavior increases.
(Min:9; Max:36)
|
4 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parents' knowledge points on digital games
Time Frame: 4 months
|
Evaluation of parents' knowledge scores about digital games
|
4 months
|
|
Families' Knowledge, Behavior and Problems Related to Digital Games Evaluation Form scores
Time Frame: 4 months
|
Evaluation of the scores obtained by parents from the form in the dimensions of "controlling their children's digital games", "protecting them from the harms of digital games", "limiting their digital games", "forcefully controlling (punishing) digital games", "guiding digital games".
|
4 months
|
|
Problems that parents have with their children due to digital games
Time Frame: 4 months
|
Evaluation of the problems parents experience with their children due to digital games
|
4 months
|
|
children's digital gaming time
Time Frame: 4 months
|
Evaluation of children's digital game playing time
|
4 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Sümbüle Köksoy Vayısoğlu, Mersin University Faculty of Nursing
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)
December 1, 2019
Primary Completion (Anticipated)
July 31, 2023
Study Completion (Anticipated)
January 1, 2024
Study Registration Dates
First Submitted
November 6, 2022
First Submitted That Met QC Criteria
November 18, 2022
First Posted (Actual)
November 30, 2022
Study Record Updates
Last Update Posted (Actual)
March 27, 2023
Last Update Submitted That Met QC Criteria
March 23, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MMUTLU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Will be shared after the completion of the research reports.
IPD Sharing Time Frame
It can be used for two years after the research reports are uploaded.
IPD Sharing Access Criteria
To be doing research on digital addictions.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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