- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05725330
The Effect of Gamification on Patients With Type 2 Diabetes
The Effect of Gamification on Disease Self-Management and Glycemic Control in Patients With Type 2 Diabetes
Study Overview
Status
Intervention / Treatment
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 Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Pelin ILHAN, MSc
- Phone Number: +905312711494
- Email: pelinilhan.54@hotmail.com
Study Contact Backup
- Name: Havva SERT, PhD
- Phone Number: +905422512100
- Email: hsert@sakarya.edu.tr
Study Locations
-
-
Sisli
-
Istanbul, Sisli, Turkey, 34360
- Recruiting
- Pelin ILHAN
-
Contact:
- Pelin ILHAN, MSc
- Phone Number: +905312711494
- Email: pelinilhan.54@hotmail.com
-
Contact:
- Havva SERT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: SUPPORTIVE_CARE
- Allocation: RANDOMIZED
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / 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.
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
self-management scale
Time Frame: 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.
|
Change between the first day and the sixth week of the study
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
glycemic control (HbA1c)
Time Frame: 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. |
Change between day one and week 6 of the study
|
|
anthropometric measurements (Body Mass Index)
Time Frame: 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). |
The change between the first day and the sixth week of the study
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ANTICIPATED)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
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
- SakaryaU.
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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