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Digital Integrated Healthcare Platform in Patients With Type 2 Diabetes

Primary Purpose

Type 2 Diabetes

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Digital integrated healthcare platform
Sponsored by
Samsung Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes focused on measuring Continuous glucose monitoring system, Artificial intelligence, Diabetes, Digital healthcare, Education

Eligibility Criteria

19 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Samsung Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Active Comparator

Experimental

Arm Label

Control A

Intervention B

Intervention C

Arm Description

no intervention conventional diabetes treatment and clinic visit every 3 months

apply digital integrated healthcare platform clinic visit every 3 months

apply digital integrated healthcare platform, CGMS, and medical team monitoring, and education clinic visit every 3 months

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

HbA1c
glycated hemoglobin
number of intervention for education in interventinal group C
The number of educational intervention by digital integrated healthcare platform
hypoglycemic events
the number of hypoglycemic events
adverse events
the number and types of hypoglycemic events
patient satisfaction questionnaire score
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.
body weight
body weight
BMI (body mass index)
BMI (body mass index)
body fat (%)
body fat (%)
step count
step count
burned calories
burned calories
walking distances
walking distances
intake calories
intake calories
fasting glucose level
fasting glucose level
total cholesterol level
total cholesterol level
HDL cholesterol level
HDL cholesterol level
Triglycerides level
Triglycerides level
LDL cholesterol level
LDL cholesterol level
mean glucose level by CGMS (continuous glucose monitoring system) in interventional group C
mean glucose level by CGMS in interventional group C
glycemic variability by CGMS in interventional group C
glycemic variability by CGMS in interventional group C
standard deviation by CGMS in interventional group C
standard deviation by CGMS in interventional group C
average applying time of CGMS in interventional group C
average applying time of CGMS in interventional group C
time in range of <54mg/dL by CGMS in interventional group C
time in range of <54mg/dL by CGMS in interventional group C
time in range of <70mg/dL by CGMS in interventional group C
time in range of <70mg/dL by CGMS in interventional group C
time in range of 70-180 mg/dL by CGMS in interventional group C
time in range of 70-180 mg/dL by CGMS in interventional group C
time in range of >180 mg/dL by CGMS in interventional group C
time in range of >180 mg/dL by CGMS in interventional group C
time in range of >250 mg/dL by CGMS in interventional group C
time in range of >250 mg/dL by CGMS in interventional group C

Full Information

First Posted
November 8, 2019
Last Updated
January 14, 2020
Sponsor
Samsung Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04161170
Brief Title
Digital Integrated Healthcare Platform in Patients With Type 2 Diabetes
Official Title
Validation of Diabetes Management Effectiveness of Digital Integrated Healthcare Platform Utilizing AI-based Dietary Management Solution and Real-time Continuous Glucose Monitoring System
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 20, 2019 (Actual)
Primary Completion Date
August 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Samsung Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
Continuous glucose monitoring system, Artificial intelligence, Diabetes, Digital healthcare, Education

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Control group A: no intervention Interventional group B: digital integrated healthcare platform Interventional group C: digital integrated healthcare platform + CGMS apply + medical team monitoring + educational intervation
Masking
None (Open Label)
Allocation
Randomized
Enrollment
294 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control A
Arm Type
No Intervention
Arm Description
no intervention conventional diabetes treatment and clinic visit every 3 months
Arm Title
Intervention B
Arm Type
Active Comparator
Arm Description
apply digital integrated healthcare platform clinic visit every 3 months
Arm Title
Intervention C
Arm Type
Experimental
Arm Description
apply digital integrated healthcare platform, CGMS, and medical team monitoring, and education clinic visit every 3 months
Intervention Type
Device
Intervention Name(s)
Digital integrated healthcare platform
Intervention Description
Digital Integrated Healthcare Platform Utilizing AI-based Dietary Management Solution and Real-time Continuous Glucose Monitoring system
Primary Outcome Measure Information:
Title
Change of HbA1c (glycated hemoglobin) at 6months from baseline
Description
Change of HbA1c (glycated hemoglobin) at 6months from baseline
Time Frame
Change of HbA1c (glycated hemoglobin) at 6months from baseline
Secondary Outcome Measure Information:
Title
HbA1c
Description
glycated hemoglobin
Time Frame
glycated hemoglobin at baseline, 3, 6, 12 months
Title
number of intervention for education in interventinal group C
Description
The number of educational intervention by digital integrated healthcare platform
Time Frame
number of intervention for education in interventinal group C at baseline, 3, 6, 12 months
Title
hypoglycemic events
Description
the number of hypoglycemic events
Time Frame
hypoglycemic events at baseline, 3, 6, 12 months
Title
adverse events
Description
the number and types of hypoglycemic events
Time Frame
adverse events at baseline, 3, 6, 12 months
Title
patient satisfaction questionnaire score
Description
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.
Time Frame
patient satisfaction questionnaire score at baseline, 3, 6, 12 months
Title
body weight
Description
body weight
Time Frame
body weight at baseline, 3, 6, 12 months
Title
BMI (body mass index)
Description
BMI (body mass index)
Time Frame
BMI at baseline, 3, 6, 12 months
Title
body fat (%)
Description
body fat (%)
Time Frame
body fat (%) at baseline, 3, 6, 12 months
Title
step count
Description
step count
Time Frame
average step count at baseline, 3, 6, 12 months
Title
burned calories
Description
burned calories
Time Frame
average burned calories at baseline, 3, 6, 12 months
Title
walking distances
Description
walking distances
Time Frame
average walking distances at baseline, 3, 6, 12 months
Title
intake calories
Description
intake calories
Time Frame
intake calories at baseline, 3, 6, 12 months
Title
fasting glucose level
Description
fasting glucose level
Time Frame
average fasting glucose level at baseline, 3, 6, 12 months
Title
total cholesterol level
Description
total cholesterol level
Time Frame
total cholesterol level at baseline, 3, 6, 12 months
Title
HDL cholesterol level
Description
HDL cholesterol level
Time Frame
HDL cholesterol level at baseline, 3, 6, 12 months
Title
Triglycerides level
Description
Triglycerides level
Time Frame
Triglycerides level at baseline, 3, 6, 12 months
Title
LDL cholesterol level
Description
LDL cholesterol level
Time Frame
LDL cholesterol level at baseline, 3, 6, 12 months
Title
mean glucose level by CGMS (continuous glucose monitoring system) in interventional group C
Description
mean glucose level by CGMS in interventional group C
Time Frame
mean glucose level by CGMS at baseline, 3, 6, 12 months
Title
glycemic variability by CGMS in interventional group C
Description
glycemic variability by CGMS in interventional group C
Time Frame
glycemic variability by CGMS at baseline, 3, 6, 12 months
Title
standard deviation by CGMS in interventional group C
Description
standard deviation by CGMS in interventional group C
Time Frame
standard deviation by CGMS at baseline, 3, 6, 12 months
Title
average applying time of CGMS in interventional group C
Description
average applying time of CGMS in interventional group C
Time Frame
average applying time of CGMS at baseline, 3, 6, 12 months
Title
time in range of <54mg/dL by CGMS in interventional group C
Description
time in range of <54mg/dL by CGMS in interventional group C
Time Frame
time in range of <54mg/dL by CGMS at baseline, 3, 6, 12 months
Title
time in range of <70mg/dL by CGMS in interventional group C
Description
time in range of <70mg/dL by CGMS in interventional group C
Time Frame
time in range of <70mg/dL by CGMS at baseline, 3, 6, 12 months
Title
time in range of 70-180 mg/dL by CGMS in interventional group C
Description
time in range of 70-180 mg/dL by CGMS in interventional group C
Time Frame
time in range of 70-180 mg/dL by CGMS at baseline, 3, 6, 12 months
Title
time in range of >180 mg/dL by CGMS in interventional group C
Description
time in range of >180 mg/dL by CGMS in interventional group C
Time Frame
time in range of >180 mg/dL by CGMS at baseline, 3, 6, 12 months
Title
time in range of >250 mg/dL by CGMS in interventional group C
Description
time in range of >250 mg/dL by CGMS in interventional group C
Time Frame
time in range of >250 mg/dL by CGMS at baseline, 3, 6, 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jae Hyeon Kim, MD PhD
Phone
+82-2-3410-1580
Email
jaehyeonmd.kim@samsung.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jae Hyeon Kim, MD PhD
Organizational Affiliation
Samsung Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
ZIP/Postal Code
135-710
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jae Hyeon Kim, M.D.,Ph. D
Phone
82-2-3410-1580
Email
jaehyeonmd.kim@samsung.com

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32650771
Citation
Park SW, Kim G, Hwang YC, Lee WJ, Park H, Kim JH. Validation of the effectiveness of a digital integrated healthcare platform utilizing an AI-based dietary management solution and a real-time continuous glucose monitoring system for diabetes management: a randomized controlled trial. BMC Med Inform Decis Mak. 2020 Jul 10;20(1):156. doi: 10.1186/s12911-020-01179-x.
Results Reference
derived

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Digital Integrated Healthcare Platform in Patients With Type 2 Diabetes

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