Type 2 Diabetes Mellitus Clinical Trial
Official title:
A Pilot Study On The Effectiveness Of Using Automated Mobile Phone Text Messaging In Improving Glycaemic Control Among Newly Detected Type 2 Diabetic Patients
NCT number | NCT02643277 |
Other study ID # | IDRFARH001 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 2014 |
Est. completion date | December 2018 |
In India, the high diabetes prevalence and cost of its management relative to their personal income render the country an appropriate environment to seek and test new, less expensive aids to care. Education and motivation to induce behavioural modification, are important components of care. Conventional diabetes education programmes involving personal contact methods are useful but expensive. Compliance with medications is also important and there are data to suggest that compliance is low in people with established type 2 diabetes (there is little information on those with recently diagnosed disease). Mobile phones could provide an inexpensive and scaleable delivery vehicle for components of care. There are now more than 5 billion wireless subscribers and 70% of them live in low and middle income countries. Mobile phone ownership is high in India and an increasing proportion now has Mobile phones and/or home computers. The investigators plan a clinical trial in India to assess whether there is benefit from an enhanced text message intervention delivered by mobile phone in people newly diagnosed with Type 2 diabetes. The message content will be directed to behavioural modification, as with our diabetes prevention studies, and will attempt to improve compliance with drug therapy and other aspects of care, as with our studies in people with established diabetes. The investigators shall compare effects on glycaemia, other cardiovascular risk factors, lifestyle behaviour and quality of life, with those observed in people with type 2 diabetes receiving standard care.
Status | Completed |
Enrollment | 244 |
Est. completion date | December 2018 |
Est. primary completion date | April 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 60 Years |
Eligibility |
Inclusion Criteria: 1. Newly diagnosed Type 2 Diabetes Mellitus patients not receiving any medication for diabetes. 2. Patients who consent to participate in the study 3. Both sexes of age = 20 and = 60 years. 4. Having an HbA1c level of = 6.5 % (48 mmol/mol) on diagnosis 5. Willing to report periodically for investigations during the study period 6. Ability to read and understand messages. Exclusion Criteria: 1. Type 1 Diabetes 2. Major illness - such as Cancer, Cardiovascular Disease, Chronic liver or kidney disease on diagnosis of diabetes. 3. Disorders with cognitive impairment, severe depression or mental imbalance. 4. Physical disability that would prevent regular physical activity. 5. Participants unwilling to participate in the study. 6. Participants who do not possess a mobile phone. 7. Participants not able to read and understand SMS. 8. Participants below the age of 20 years and above the age of 60 years. |
Country | Name | City | State |
---|---|---|---|
India | Dr.A.Ramachandran's Diabetes Hospitals | Chennai | Tamil Nadu |
Lead Sponsor | Collaborator |
---|---|
India Diabetes Research Foundation & Dr. A. Ramachandran's Diabetes Hospitals |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Comparison of the glycaemic outcome measured as improvement in HbA1c (= 7.0% (53mmol/mol)) in the intervention group in comparison with the conventional care. | 2 years | ||
Secondary | Changes in body mass index | We are assessing the changes in BMI not the changes in weight & height and the unit for BMI is Kg/m2. It is a single unit of measurement calculated by patients weight and Height. | Baseline and 2 years | |
Secondary | Changes in blood pressure | Baseline and 2 years | ||
Secondary | Changes in fasting and postprandial plasma glucose | Baseline and 2 years | ||
Secondary | Changes in lipid profile | Baseline and 2 years | ||
Secondary | Improvement in quality of life | Scale | Baseline and 2 years | |
Secondary | Improvement in acceptance of this strategy as an educative tool by the patients | Questionnaire | Baseline and 2 years | |
Secondary | Adherence to the prescription | Analysis | Baseline and 2 years |
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