Status:
UNKNOWN
Use of the MyDose Coach Digital Tool for Self-titration of Insulin in Patients With Type 2 Diabetes
Lead Sponsor:
Hospital Universitario Dr. Jose E. Gonzalez
Collaborating Sponsors:
Hospital Clinica Nova
Conditions:
Diabetes Mellitus, Type 2
Eligibility:
All Genders
18-75 years
Phase:
NA
Brief Summary
Scientific studies show that the introduction of digital tools led to: Significant improvement in glycemic control, greater patient satisfaction, reduction of emotional burden, reduction of fear of hy...
Detailed Description
The maximum study duration will be 29 weeks per patient that will consist of a 12-week screening period, a 16-week treatment period, and 1-week follow-up period.
Eligibility Criteria
Inclusion
- Have type 2 diabetes
- Greater than 18 years and up to 75 years of age
- Use of basal insulin once a day or candidate for basal insulin once a day based on% HbA1c according to international guidelines and doctor's criteria
- HbA1c \> 7% in patients aged 18 to 65 years
- HbA1c \> 7.5% in patients older than 65 years
- Patients who use basal insulin twice a day or premix with diagnosed hypoglycemia and who are candidates for switching from therapy to a basal insulin of one application per day
- Have a Smartphone
- Informed consent signature
Exclusion
- Refuse to participate in the study.
- Age younger than 18 years old and over 75 years old.
- Diabetes type 1 or gestational (other than type 2 diabetes mellitus).
- Patients with the following chronic complications of diabetes: retinopathy and chronic kidney disease with a glomerular filtration rate \<30 ml / min.
- The MyDose Coach tool is not appropriate for the patient or the use of the application is contraindicated (in the opinion of the Researcher, for example, patients with terminal illness, patients with cognitive or neurological disorders that are detailed below, patients who live alone and they do not have support from the family, patients with carpal tunnel who are not recommended to use a mobile phone, patients with musculoskeletal injuries in their hands, etc.)
- Patients who use insulin during the meal (short-acting analogue, regular human insulin or insulin premix) for more than 10 days in the last 3 months before the screening visit.
- Patients with severe hypoglycemia in the last 90 days.
- Hospitalization in the last 30 days (whatever the reason for hospitalization) In the last 3 months prior to the screening period: history of myocardial infarction, unstable angina, acute coronary syndrome, revascularization procedure, cerebrovascular accident requiring hospitalization.
- Severe or uncontrolled congestive heart failure (functional classification III and IV of the New York Heart Association \[NYHA\]).
- Use of systemic glucocorticoids (excluding topical application or inhaled forms) for a week or more within 90 days prior to the time of the test.
- Unable to meet specific protocol requirements (for example, inability to perform blood glucose measurements, administer your own insulin dose, or consider it unlikely that you will administer the titration safely according to your physician's guidance).
- Patients with cognitive disorders, dementia or any neurological disorder that affects the patient's ability to participate in the study, including the inability to understand the requirements of the study or to provide complete information about the adverse symptoms.
- Pregnant or breast-feeding women or women who intend to become pregnant during the study period.
Key Trial Info
Start Date :
August 22 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 22 2019
Estimated Enrollment :
300 Patients enrolled
Trial Details
Trial ID
NCT03775057
Start Date
August 22 2018
End Date
August 22 2019
Last Update
December 17 2018
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Clínica Nova
San Nicolás de los Garza, Nuevo León, Mexico