- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07409701
Gamification Intervertion in Children With Type 1 Diabetes
The Effect of Education Provided to Children With Type 1 Diabetes Using Gamification Methods on Health Literacy and Quality of Life: A Randomized Controlled Trial
Objective: This study aims to examine the effect of education provided through gamification methods on health literacy and quality of life in children diagnosed with type 1 diabetes (T1DM).
Materials and Methods: The study is planned as a randomized controlled trial with a pre-test-post-test, parallel design (1:1). The data for the study will be collected between January and April 2026 from patients diagnosed with type 1 diabetes mellitus at the Ankara Etlik City Hospital Pediatric-2 Endocrinology Service. The sample size has been determined to be 52 patients, with 26 in each of the experimental and control groups, based on data from similar studies in the literature. Data will be collected through individual interviews using a Personal Information Form, the Health Literacy Scale for Acute Complications of Diabetes in Children Aged 8-12 with type 1 diabetes mellitus, and the Quality of Life Scale for Children with Diabetes Mellitus. The gamified education will be provided by a researcher who has completed a 2.5-hour training program from BTK Academy. Informed Consent Forms and other forms will be completed by patients who meet the inclusion criteria and volunteer to participate. Randomization will be performed by someone other than the researcher. The experimental group will receive gamified education in addition to standard education, while the control group will receive only standard education. Data will be analyzed using the SPSS program. The research will be conducted in accordance with the principles of the Helsinki Declaration.
Findings: The findings of the study will be analyzed using SPSS after the application and data collection are completed.
Conclusion: The results of the study will be written after the application of the study and the collection of data, followed by the analysis of the data using SPSS and the determination of the findings.
Study Overview
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Gülfidan Başer
- Phone Number: 4441251-7550
- Email: gulfidan.baser@karatay.edu.tr
Study Locations
-
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Yenimahalle
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Ankara, Yenimahalle, Turkey (Türkiye)
- Recruiting
- Etlik City Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Diagnosed with type 1 diabetes
- Aged between 8 and 12 years
- Diagnosed with type 1 diabetes for at least 1 year and having received standard diabetes education
- Able to read and write
Exclusion Criteria:
- Presence of speech, hearing, or visual impairments
- Presence of any other comorbid chronic disease
- Presence of cognitive impairment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: standard
|
|
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Active Comparator: education provided through gamification methods
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This intervention will provide randomized controlled evidence on a gamified diabetes education program for children, an approach that is currently limited in Türkiye, thereby contributing to evidence-based practice.
In addition, by adopting a holistic approach that jointly evaluates health literacy and psychological symptoms, the program aims not only to improve knowledge but also to enhance quality of life through an innovative and effective educational model.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health Literacy Scale for Acute Complications of Diabetes in Children Aged 8-12
Time Frame: Through study completion, an average of 1 year
|
The scale developed by Çövener and Yeşil (2024) consists of 18 items and three subscales.
A highly significant positive correlation was found between the total scale score and the subfactors of knowledge about acute complications of diabetes, interpretation of encountered problems, and healthy lifestyle behaviors (p=0.000).
In other words, as the total scale score increases, the subfactor scores also increase.
|
Through study completion, an average of 1 year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of Life Scale for Children with Diabetes Mellitus
Time Frame: Through study completion, an average of 1 year
|
A linear conversion is applied in the calculation of the total score on the scale, converting it to a score between 0 and 100.
If the answer to the question is marked as never, it receives 100 points; if marked as rarely, it receives 75 points; if marked as sometimes, it receives 50 points; if marked as often, it receives 25 points; and if marked as almost always, it receives 0 points.
The higher the total score, the better the perceived health-related quality of life.
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Through study completion, an average of 1 year
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Collaborators and Investigators
Sponsor
Collaborators
Publications and helpful links
General Publications
- Akın, B., & Koçoğlu, D. (2017). Randomize kontrollü deneyler. *Hacettepe Üniversitesi Hemşirelik Fakültesi Dergisi*, 4(1), 73-92. American Diabetes Association. (2023). Standards of medical care in diabetes-2023. *Diabetes Care*, 46(Supplement\_1), S1-S291. Altundağ, S. (2018). Tip 1 diyabetli çocukların hastalığa uyumunda eğitimin ve sosyal desteğin etkisi. *Pamukkale Tıp Dergisi*, 11(2):137-144. Akyol Güner, T., Kuzu, A., & Bayraktaroğlu, T. (2020). Diyabetli bireylerde sağlık okuryazarlığı ve akılcı ilaç kullanımı arasındaki ilişki. *Turkish Journal of Diabetes and Obesity*, 4(3), 214-223. Ayar, D. (2012). *Diabetes Mellitus'lu çocuklarda yaşam kalitesi ölçeğinin geçerlik ve güvenirlik çalışması*. Yüksek lisans tezi, Dokuz Eylül Üniversitesi, Sağlık Bilimleri Enstitüsü, İzmir. [YÖK Ulusal Tez Merkezi](https://tez.yok.gov.tr/UlusalTezMerkezi/tezDetay.jsp?id=MEPAo2hK_UTZZs2oWMCStw&no=u1Mx6E6BUBcEGeGf10E0eg) Ayar, D., & Öztürk, C. (2015). Ebeveyn perspektifiyle pediatrik yaşam kalitesi envanteri diyabet modülünün Türkçe geçerlik güvenirlik çalışması. *Hemşirelikte Araştırma Geliştirme Dergisi*, 17(2/3), 1-9. Baştopçu, Ö., Arslan, S., Arslanoğlu, İ. (2021). Tip 1 diyabetli adölesanların uyku ve yaşam kalitesi ile psikolojik sağlamlık düzeyleri arasındaki ilişki. *International Anatolia Academic Online Journal Health Sciences*, 7(2). Bilgin, M., Yılmaz, A., & Kaya, S. (2020). Kronik hastalıklarda yaşam kalitesine genel bakış. *Erciyes Üniversitesi Sağlık Bilimleri Dergisi*, 9(1), 1-10. Bujanda, A., Bujanda, E. (2022). DIABESCAPE: An innovative educational project on diabetes. *Endocrinologia Diabetes Nutricion*, 69(6), 392-400. Çakmak, M. A., Simzari, W. (2024). Sağlıklı beslenmenin öğretilmesi ile ilgili bir oyunlaştırma modeli önerisi. *IGUSABDER*, 931-940. Delibaş, L., Erci, B. (2021). Sosyal bilişsel kuram temelli eğitimle tip 1 diyabetli çocukların hastalık yönetiminin desteklenmesi. *TJFMPC*, 15(2):404-13. Demir, G., Akcay, N. (2022). Diabetes education in child
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025/061 (Comité de Ética de la Investigación de A Coruña-Ferrol)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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