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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03273140 |
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Date of registration:
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26/08/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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The Effectiveness of Gamification Diabetes Education Program for Poorly Controlled Type 2 Diabetic Patients
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Scientific title:
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The Effectiveness of Gamification Diabetes Education Program for Poorly Controlled Type 2 Diabetic Patients: A Randomised Controlled Trial. |
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Date of first enrolment:
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March 1, 2017 |
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Target sample size:
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158 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03273140 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Other. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Singapore
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. Patient who is clinically diagnosed with type 2 diabetes mellitus.
2. Patient with HbA1C value > 7% at least within the past two months.
3. Patient who can speak and understand English.
4. Patient of age 21 to 75 years old.
5. Patient with either a smartphone or i-pad/ tablet.
Exclusion Criteria:
1. Pregnant patient.
2. Patient diagnosed to have a terminal illness.
3. Patient with cognitive impairment.
4. Patient with end-stage renal failure (ESRF).
Age minimum:
21 Years
Age maximum:
75 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Diabetic Patients, Gamification, Diabetic Education
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Intervention(s)
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Device: Gamification Diabetes Education Program (GDEP)
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Primary Outcome(s)
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Better HbA1c values
[Time Frame: Every three months up to 24th week (0 week as baseline, 12th week and 24th week)]
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Better Sense of Coherence
[Time Frame: Every three months up to 24th week (0 week as baseline, 12th week and 24th week)]
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Better Self-efficacy
[Time Frame: Every three months up to 24th week (0 week as baseline, 12th week and 24th week)]
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Secondary Outcome(s)
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Better Quality of life
[Time Frame: Every three months up to 24th week (0 week as baseline, 12th week and 24th week)]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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