The Effect of Gamification on Patients With Type 2 Diabetes

Sponsor
Sakarya University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05725330
Collaborator
(none)
88
1
2
10.1
8.7

Study Details

Study Description

Brief Summary

Diabetes is a broad-spectrum metabolic disorder that causes a defect in the organism's carbohydrate, fat, and protein metabolism processes due to insulin deficiency or impaired insulin effect. Diabetes requires continuous medical care and causes chronic, severe mortality and morbidity. More than 90% of all people with diabetes worldwide suffer from Type 2 DM. Diabetes self-management includes self-monitoring of blood glucose levels, knowing and managing the symptoms of hypoglycemia and hyperglycemia, adherence to diet, physical exercise, and diabetic foot care. Considering the high prevalent and undesirable consequences of diabetes in the world, it is necessary to benefit from new educational technologies and tools. One of these technologies is gamification, which increases the quality of education as an effective educational tool, creates motivation and enthusiasm, and develops a sense of competition in the target audience. This study plans to develop a game that will include virtual coaching to increase the self-management and glycemic control of patients with type 2 diabetes.

Condition or Disease Intervention/Treatment Phase
  • Other: Gamification and education with mobile game application
N/A

Detailed Description

The research will be carried out in two stages. In Stage 1, the game will be developed; The developed game's effectiveness will be evaluated in the 2nd stage by testing it. The game's content will include healthy nutrition, exercise, foot care, insulin use, and hypoglycemia management. When the games are completed, the virtual coach will step in, and the participants will be given motivational feedback. The game developed will be evaluated by the patients in the second stage with a two-week pilot period. It will be updated according to the feedback received. The final version of the game will be passed forward to the implementation phase. Individuals who are willing to participate in the study coming to Prof. Dr. Cemil Tascioglu City Hospital Diabetes Polyclinic will be randomly assigned to the intervention and control groups. A total of 88 patients (44 controls - 44 experiments) are planned to be recruited. In the first interview with the individuals in the intervention group, Within the scope of the pretest, the "Personal Information Form," "Anthropometric Measurement Form," "Metabolic Control Variables Form," and "Diabetes Self-Management Scale" will be used for evaluation. Outpatient appointment dates of the sixth week of the intervention program, "Anthropometric Measurement Form," "Metabolic Control Variables Form," and "Diabetes Self-Management Scale" forms will be used with patients for the final evaluation within the scope of the posttest.

In the first meeting with the individuals in the control group, explanations about the research will be made. After their written consent is obtained at the first interview and within the scope of the pretest, the "Personal Information Form," "Anthropometric Measurement Form," "Metabolic Control Variables Form," and "Diabetes Self-Management Scale" will be used for evaluation. At the end of the sixth week of the study, when they come in for their outpatient clinic appointments, as a part of the posttest, "Anthropometric Measurement Form," "Metabolic Control Variables Form," and "Diabetes Self-Management Scale" forms will be used for the final evaluation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
88 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Gamification on Disease Self-Management and Glycemic Control in Patients With Type 2 Diabetes
Anticipated Study Start Date :
Feb 25, 2023
Anticipated Primary Completion Date :
Sep 17, 2023
Anticipated Study Completion Date :
Dec 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

Application of data collection forms for the initial evaluation. Teaching the use of mobile games, monitoring the use of mobile games in the experimental group by the researcher for six weeks, and applying data collection forms to the patients in the sixth week.

Other: Gamification and education with mobile game application
This study aimed to provide self-care management by playing mobile games to patients with type 2 diabetes.

No Intervention: Control Group

Application of data collection forms for the initial evaluation. Application of data collection forms to the patients in the sixth week. No intervention will be made to the patients in the control group other than the routine education given in the diabetes outpatient clinic.

Outcome Measures

Primary Outcome Measures

  1. self-management scale [Change between the first day and the sixth week of the study]

    Determining whether or not the disease self-management scale scores in patients with Type 2 DM using the developed mobile game application increased at the end of the 6 weeks period. A minimum of 0 and a maximum of 10 points are obtained on the scale. If an item is skipped, it is evaluated as -3 points. Diabetes self-management increases as the score get closer to 10.

Secondary Outcome Measures

  1. glycemic control (HbA1c) [Change between day one and week 6 of the study]

    The effect that the mobile game application developed imposes on glycemic control in patients with Type 2 DM at six weeks compared to baseline. The effect of the patient's HbA1c tests on the 6th week compared to the baseline. Blood test (HbA1c) will be performed during the outpatient follow-up at the first and sixth weeks.

  2. anthropometric measurements (Body Mass Index) [The change between the first day and the sixth week of the study]

    The effects on anthropometric measurements in patients with Type 2 DM using the mobile game application developed compared to baseline at week 6. The effect on the patient's Body Mass Index compared to baseline at week 6. The researcher will measure it. Body Mass Index is calculated by dividing the person's weight in kilograms by the square of the person's height in meters (kg/m²).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Two years or more with a diagnosis of Type 2 DM

  • Patients using Insulin or Insulin and Oral Antidiabetic

  • No sensory loss, such as vision and hearing loss,

  • Having internet access and being able to use it,

  • Ability to use a mobile phone with an Android or IOS (iPhone OS) operating system

  • Patients who agreed to participate in the study

Exclusion Criteria:
  • Patients diagnosed with Type 1 DM and Gestational DM.

  • Visual and auditory loss,

  • Individuals without internet access

  • Unable to communicate

Contacts and Locations

Locations

Site City State Country Postal Code
1 Pelin ILHAN Istanbul Sisli Turkey 34360

Sponsors and Collaborators

  • Sakarya University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sakarya University
ClinicalTrials.gov Identifier:
NCT05725330
Other Study ID Numbers:
  • SakaryaU.
First Posted:
Feb 13, 2023
Last Update Posted:
Feb 13, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 13, 2023