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Glycemic Control Using Mobile-based Intervention in Patients With Diabetes Undergoing Coronary Artery Bypass to Promote Self-management (GUIDEME)

Primary Purpose

Coronary Artery Disease, Coronary Artery Bypass, Diabetes Mellitus

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Smartphone Application
Sponsored by
China National Center for Cardiovascular Diseases
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Coronary Artery Disease focused on measuring Coronary Artery Disease, Coronary Artery Bypass Grafting, Diabetes Mellitus, Smartphone Application, Postoperative Management

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnose with type 2 diabetes before this administration;
  • Postoperative patients undergoing CABG in this hospitalization;

Exclusion Criteria:

  • Die before discharge;
  • Disability of reading, vision or hearing which leads to disability of using smartphone;
  • Cognitive communication impairments or communication disorder;
  • Unable to use smartphone.

Sites / Locations

  • Chinese Academy of Medical Science,Fuwai Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention-Smartphone Application

Control

Arm Description

Patients will install a smartphone application that custom-developed for the study and learn to use it with the help of researchers. The application will have the following functions: 1) providing health education information about glycemic control, postoperative management and important of drug compliance; 2) providing alert & record service on patients' DM and CAD medication treatment; 3) aiding patients to conduct self-evaluate by providing questionnaire about patients' recent basic health parameters on times. The information will be interpreted automatically by application and brief feedback will be provided to patients; 4) recording patients' fasting plasma glucose value that input by patients and generate a recent glycemic control report.

Patients will receive no additional intervention from researchers except the usual care provided by hospital.

Outcomes

Primary Outcome Measures

Change in glucose level measured by HbA1C level
We will measured the change in glucose level from baseline to 6 months.

Secondary Outcome Measures

The incidence of all-cause death
We will measure the incidence of all-cause death at 6 months.
The incidence of major adverse cardiovascular events(MACE)
We will measure the incidence of major adverse cardiovascular events(MACE) at 6 months.
EQ-5D
We will measure the change in EQ-5D health survey 6 months postoperatively.
Medication adherence
Medication adherence is collected by a self-reported questionnaire including two questions: 1) have you ever forget to take your medication? If so, how often will you describe? 2) have you ceased to take any medication? If so, does it ceased as prescribed by doctor? Question 1 has four option if patients choose yes: 1) I hardly forget to take my medicine; 2) I forget to take my medicine monthly; 3) I forget to take my medicine every week; 4) I hardly take any medicine.
Status of the graft vessels
We will measure the status of the graft vessels by coronary CT angiography at 6 months.
blood pressure
We will document blood pressure at 6 months postoperatively.
blood glucose
We will document blood glucose at 6 months postoperatively.
low density lipoprotein
We will document low density lipoprotein at 6 months postoperatively.

Full Information

First Posted
October 30, 2019
Last Updated
January 18, 2023
Sponsor
China National Center for Cardiovascular Diseases
Collaborators
Chinese Academy of Medical Sciences, Fuwai Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04192409
Brief Title
Glycemic Control Using Mobile-based Intervention in Patients With Diabetes Undergoing Coronary Artery Bypass to Promote Self-management
Acronym
GUIDEME
Official Title
Glycemic Control Using Mobile-based Intervention in Patients With Diabetes Undergoing Coronary Artery Bypass to Promote Self-management
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
January 1, 2020 (Actual)
Primary Completion Date
April 1, 2022 (Actual)
Study Completion Date
June 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
China National Center for Cardiovascular Diseases
Collaborators
Chinese Academy of Medical Sciences, Fuwai Hospital

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
The study is a two-arm parallel, randomized clinical trial. The purpose of the study is to evaluate the effectiveness and feasibility of using high-quality medication reminder smartphone application as a tool for secondary prevention in patients undergone CABG with DM, including the change in quality of life, medication adherence improvement and clinical outcome. The participants will be randomized into intervention and control groups in a 1:1 ratio. The intervention group will receive information of secondary prevention of CHD and medication alarm using a specific smartphone application, while the control group will receive usual care.
Detailed Description
Objective: this study designed to evaluate the effectiveness and feasibility of using high-quality medication reminder smartphone application as a tool for secondary prevention in patients undergone CABG with DM, including the change in quality of life, medication adherence improvement and clinical outcome. Study design: the study is a two-arm, parallel, randomized clinical trial. Patients will be eligible if they have undergone CABG at this admission, have a history of diabetes mellitus, have the capability of reading and using smartphone application, and are able to provide informed consent. Patients will be excluded if they do not have smartphone. The eligible participants will be allocated into intervention and control groups in a 1:1 ratio randomly. The intervention group will receive intervention of smartphone application in addition to usual care, while the control group will receive usual care. All the participants will be followed up for 6 months. Study intervention: participants in the intervention group will install a specific costume smartphone application, which will send health education information, medication alarm and risk factor questionnaire at a fixed frequency to aid patients' self-evaluation, recording patients' recent fast plasma glucose value in addition to usual care. Outcome measures: The primary endpoint is the change in glycemic hemoglobin (HbA1C). Secondary endpoints include MACCE, medication adherence, quality of life and status of graft vessel. Statistical analysis: Evaluation will be carried out on an intention-to-treat basis. Values of analyzed endpoints between intervention group and control group will be compared according to the analysis plan. We'll follow a prespecified analysis plan and subgroup analysis will be conducted accordingly.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Coronary Artery Bypass, Diabetes Mellitus
Keywords
Coronary Artery Disease, Coronary Artery Bypass Grafting, Diabetes Mellitus, Smartphone Application, Postoperative Management

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1038 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention-Smartphone Application
Arm Type
Experimental
Arm Description
Patients will install a smartphone application that custom-developed for the study and learn to use it with the help of researchers. The application will have the following functions: 1) providing health education information about glycemic control, postoperative management and important of drug compliance; 2) providing alert & record service on patients' DM and CAD medication treatment; 3) aiding patients to conduct self-evaluate by providing questionnaire about patients' recent basic health parameters on times. The information will be interpreted automatically by application and brief feedback will be provided to patients; 4) recording patients' fasting plasma glucose value that input by patients and generate a recent glycemic control report.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Patients will receive no additional intervention from researchers except the usual care provided by hospital.
Intervention Type
Behavioral
Intervention Name(s)
Smartphone Application
Intervention Description
Patients will use a smartphone application contain the following functions: providing health education information about DM and CAD, reminding patients to take medicine on time by alarm, recording patients' recent fast plasma glucose value.
Primary Outcome Measure Information:
Title
Change in glucose level measured by HbA1C level
Description
We will measured the change in glucose level from baseline to 6 months.
Time Frame
Baseline; 6 months
Secondary Outcome Measure Information:
Title
The incidence of all-cause death
Description
We will measure the incidence of all-cause death at 6 months.
Time Frame
6 months
Title
The incidence of major adverse cardiovascular events(MACE)
Description
We will measure the incidence of major adverse cardiovascular events(MACE) at 6 months.
Time Frame
6 months
Title
EQ-5D
Description
We will measure the change in EQ-5D health survey 6 months postoperatively.
Time Frame
6 months
Title
Medication adherence
Description
Medication adherence is collected by a self-reported questionnaire including two questions: 1) have you ever forget to take your medication? If so, how often will you describe? 2) have you ceased to take any medication? If so, does it ceased as prescribed by doctor? Question 1 has four option if patients choose yes: 1) I hardly forget to take my medicine; 2) I forget to take my medicine monthly; 3) I forget to take my medicine every week; 4) I hardly take any medicine.
Time Frame
6 months
Title
Status of the graft vessels
Description
We will measure the status of the graft vessels by coronary CT angiography at 6 months.
Time Frame
6 months
Title
blood pressure
Description
We will document blood pressure at 6 months postoperatively.
Time Frame
6 months
Title
blood glucose
Description
We will document blood glucose at 6 months postoperatively.
Time Frame
6 months
Title
low density lipoprotein
Description
We will document low density lipoprotein at 6 months postoperatively.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnose with type 2 diabetes before this administration; Postoperative patients undergoing CABG in this hospitalization; Exclusion Criteria: Die before discharge; Disability of reading, vision or hearing which leads to disability of using smartphone; Cognitive communication impairments or communication disorder; Unable to use smartphone.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wei Feng, MD, PhD
Organizational Affiliation
Chinese Academy of Medical Sciences, Fuwai Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chinese Academy of Medical Science,Fuwai Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100037
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Glycemic Control Using Mobile-based Intervention in Patients With Diabetes Undergoing Coronary Artery Bypass to Promote Self-management

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