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Digital Integrated Healthcare Platform in Patients With Type 2 Diabetes

Not Applicable
Conditions
Type 2 Diabetes
Interventions
Device: Digital integrated healthcare platform
Registration Number
NCT04161170
Lead Sponsor
Samsung Medical Center
Brief Summary

In this three multicenter clinical trial, investigators will study the efficacy of digital integrated healthcare platform and CGMS (continuous glucose monitoring system) on diabetes management in patients with Type 2 diabetes. The platform is based on monitoring and intervention by medical staff using AI (aritificial intelligence)-based diet management solution.

The study group includes 3 groups; a total of 294 participants with 1:1:1 randomized allocation: Control group A (no intervention and conventional diabetes management with regular outpatiant clinic visit every 3 months), Interventional group B (applying digital integrated healthcare platform by themselves, no monitoring and intervention by medical staff), and Interventional group C (applying digital integrated healthcare platform based on monitoring and intervention by medical staff using AI-based diet management solution and applying CGMS).

This parallel study will be conducted for 48 weeks.

Detailed Description

The reason why it is difficult to improve the lifestyle of patients with diabetes using existing digital healthcare applications (apps) is that there is a limit of sustainability that most people do not continue to use digital healthcare apps, thus, it can be possible only with monitoring and intervention by medical staff.

Not only users, but also medical staff can access integrated biometric data on the digital integrated healthcare platform so that individual patient-specific management systems that monitor and intervene can continuously motivate patients to manage themselves. Also, it could be a prerequisite for the successful management of patients with diabetes using digital healthcare apps, many existing apps have been identified as failure cases in previous studies. In this clinical trial, investigators will study the efficacy of digital integrated healthcare platform based on monitoring and intervention by medical staff using AI (aritifical intelligence)-based diet management solution.

In addition, in this clinical trial, the latest medical device, real-time continuous glucose monitoring system (CGMS) will be applied to monitor blood glucose levels. It has been reported that glucose level is well controlled when the number of self blood glucose measurement is performed frequently, but in practice, patients have time and space limitation in self blood glucose measurement, and it is difficult to change the management pattern of patients by encouraging self blood glucose measurement. Therefore, by applying a CGMS every three months, not only the patient but also the medical staff can access the 24-hour blood glucose values, and can actively participate in the blood sugar management of the patients. Therefore, investigators plan to conduct clinical trial using digital integrated healthcare platform using AI-based diet management solution and real-time CGMS

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
294
Inclusion Criteria
  • 19~70 aged patients with type 2 diabetes
  • Patients who have not taken diabetic medications for more than 4 weeks and patients who have taken at least one type of oral hypoglycemic agents at same dosage for more than 12 weeks
  • Those who have glycated hemoglobin within 7.0% to 8.5% within the last 3 months
  • overweight or obese: BMI (body mass index) ≥ 23 kg / m2
  • Those who have agreed to use medical record and participate research by applying the digital integrated healthcare platform
  • Those who voluntarily signed the consent form after listening the explanation of the clinical trial.
Exclusion Criteria
  • Diabetes other than type 2 diabetes, including type 1 diabetes and gestational diabetes
  • Those who are receiving insulin or GLP-1 agonist other than oral hypoglycemic agents
  • Uncontrolled chronic liver disease (hemochromatosis, liver cancer, autoimmune liver disease, cirrhosis of the liver, viral hepatitis-includes all A, B and C, Wilson's disease)
  • Those with acute renal failure (up to 1.5 times higher than existing serum creatinine)
  • Those with mental illness (schizophrenia, depression, bipolar disorder, etc.)
  • Those who are currently taking weight loss agents
  • Those who had alcohol or drug addiction within the last three months
  • Those who are taking medications that may affect glucose metabolism (eg, corticosteroids, immunoreactive drugs, etc.)
  • Those who are pregnant or lactating and planning to become pregnant during the clinical trial (women of childbearing age may agree to the contraceptive plan).
  • Those who are deemed inappropriate for participation in clinical trials

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention BDigital integrated healthcare platformapply digital integrated healthcare platform clinic visit every 3 months
Intervention CDigital integrated healthcare platformapply digital integrated healthcare platform, CGMS, and medical team monitoring, and education clinic visit every 3 months
Primary Outcome Measures
NameTimeMethod
Change of HbA1c (glycated hemoglobin) at 6months from baselineChange of HbA1c (glycated hemoglobin) at 6months from baseline

Change of HbA1c (glycated hemoglobin) at 6months from baseline

Secondary Outcome Measures
NameTimeMethod
burned caloriesaverage burned calories at baseline, 3, 6, 12 months

burned calories

patient satisfaction questionnaire scorepatient satisfaction questionnaire score at baseline, 3, 6, 12 months

patient satisfaction questionnaire score includes 8 questions and each question has score range 0 (min) - 6 (max). For questions number 2 and 3, higher score mean worse outcome in hypoglycemia but for the rest of questions, higher scores mean better outcome in diabetes management.

total cholesterol leveltotal cholesterol level at baseline, 3, 6, 12 months

total cholesterol level

glycemic variability by CGMS in interventional group Cglycemic variability by CGMS at baseline, 3, 6, 12 months

glycemic variability by CGMS in interventional group C

HbA1cglycated hemoglobin at baseline, 3, 6, 12 months

glycated hemoglobin

hypoglycemic eventshypoglycemic events at baseline, 3, 6, 12 months

the number of hypoglycemic events

adverse eventsadverse events at baseline, 3, 6, 12 months

the number and types of hypoglycemic events

body weightbody weight at baseline, 3, 6, 12 months

body weight

number of intervention for education in interventinal group Cnumber of intervention for education in interventinal group C at baseline, 3, 6, 12 months

The number of educational intervention by digital integrated healthcare platform

BMI (body mass index)BMI at baseline, 3, 6, 12 months

BMI (body mass index)

step countaverage step count at baseline, 3, 6, 12 months

step count

walking distancesaverage walking distances at baseline, 3, 6, 12 months

walking distances

fasting glucose levelaverage fasting glucose level at baseline, 3, 6, 12 months

fasting glucose level

body fat (%)body fat (%) at baseline, 3, 6, 12 months

body fat (%)

intake caloriesintake calories at baseline, 3, 6, 12 months

intake calories

time in range of <70mg/dL by CGMS in interventional group Ctime in range of <70mg/dL by CGMS at baseline, 3, 6, 12 months

time in range of \<70mg/dL by CGMS in interventional group C

time in range of >250 mg/dL by CGMS in interventional group Ctime in range of >250 mg/dL by CGMS at baseline, 3, 6, 12 months

time in range of \>250 mg/dL by CGMS in interventional group C

HDL cholesterol levelHDL cholesterol level at baseline, 3, 6, 12 months

HDL cholesterol level

time in range of <54mg/dL by CGMS in interventional group Ctime in range of <54mg/dL by CGMS at baseline, 3, 6, 12 months

time in range of \<54mg/dL by CGMS in interventional group C

time in range of >180 mg/dL by CGMS in interventional group Ctime in range of >180 mg/dL by CGMS at baseline, 3, 6, 12 months

time in range of \>180 mg/dL by CGMS in interventional group C

time in range of 70-180 mg/dL by CGMS in interventional group Ctime in range of 70-180 mg/dL by CGMS at baseline, 3, 6, 12 months

time in range of 70-180 mg/dL by CGMS in interventional group C

Triglycerides levelTriglycerides level at baseline, 3, 6, 12 months

Triglycerides level

LDL cholesterol levelLDL cholesterol level at baseline, 3, 6, 12 months

LDL cholesterol level

mean glucose level by CGMS (continuous glucose monitoring system) in interventional group Cmean glucose level by CGMS at baseline, 3, 6, 12 months

mean glucose level by CGMS in interventional group C

standard deviation by CGMS in interventional group Cstandard deviation by CGMS at baseline, 3, 6, 12 months

standard deviation by CGMS in interventional group C

average applying time of CGMS in interventional group Caverage applying time of CGMS at baseline, 3, 6, 12 months

average applying time of CGMS in interventional group C

Trial Locations

Locations (1)

Samsung Medical Center

🇰🇷

Seoul, Korea, Republic of

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