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Cardiovascular Health and Text Messaging-Diabetes Mellitus (CHAT-DM) Study

Primary Purpose

Coronary Artery Disease, Diabetes

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Text messaging
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, Diabetes, Text messages

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Participants with coronary artery disease defined as history of myocardial infarction and PCI
  • History of diabetes
  • Capability to read and send text messages

Exclusion Criteria:

  • Assumed poor adherence
  • Do not have an active mobile phone

Sites / Locations

  • Fuwai hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention-Text messaging

Control

Arm Description

Patients will receive regular semi-personalized text messages for 6 months. Each participants will receive 6 text messages per week, which will be sent at random times of the day (9.00am, 12noon, 4.00pm). They will receive one general messages, one hypertension message, one glucose control message, one lifestyle message, one medication adherence message and one physical activity message per week.

Participants in the control group will receive 2 thank-you messages per month and undertake routine clinical practice.

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

Change in proportion of patients achieving HbA1C<7%
We will measure the change in proportion of patients achieving HbA1C<7% from baseline to 6 months.
Change in level of fasting blood glucose (FBG)
We will measure the change in FBG level from baseline to 6 months.
Change in body mass index (BMI) according to national standards
We will measured the change in BMI from baseline to 6 months.
Change in systolic blood pressure (SBP) obtained in office during each interview
We will measured the change in SBP from baseline to 6 months.
Change in level of physical activity measured via International Physical Activity Questionnaire (IPAQ) scale
We will measure the change in IPAQ scale from baseline to 6 months.
Change in medication adherence
We will measure the change in medication adherence from baseline to 6 months.
Change in low-density lipoprotein cholesterol (LDL-C) level
We will measure the change in LDL-C level from baseline to 6 months.

Full Information

First Posted
August 24, 2016
Last Updated
May 7, 2018
Sponsor
China National Center for Cardiovascular Diseases
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1. Study Identification

Unique Protocol Identification Number
NCT02883842
Brief Title
Cardiovascular Health and Text Messaging-Diabetes Mellitus (CHAT-DM) Study
Official Title
Effectiveness of Text Messaging on Risk Factors Control and Medication Adherence Among Patients With Coronary Heart Disease and Diabetes in China: Cardiovascular Health and Text Messaging-Diabetes Mellitus (CHAT-DM) Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
August 2016 (Actual)
Primary Completion Date
November 2017 (Actual)
Study Completion Date
November 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
China National Center for Cardiovascular Diseases

4. Oversight

Data Monitoring Committee
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 of automated mobile phone text message-based intervention for secondary prevention, including lifestyles modification, medication adherence improvement and risk factors control among coronary heart disease (CHD) patients with diabetes. The participants will be randomized into intervention and control groups in a 1:1 ratio. The intervention group will receive 6 pre-designed text messages per week in addition to usual care for 6 months, while the control group will receive usual care.
Detailed Description
Objective: This study aims to evaluate the effectiveness of automated mobile phone text message-based intervention for secondary prevention, including lifestyles modification, medication adherence improvement and risk factors control among CHD patients with diabetes. We hypothesized that an intervention using mobile phone text based education and reminder can improve risk factors control and medication adherence for CHD patients. Study design: The study is a two-arm, parallel, randomized clinical trial. Patients will be eligible if they have documented CHD defined as having history of myocardial infarction and percutaneous coronary intervention (PCI), have a history of diabetes mellitus, have the capability of reading and sending short message, and are able to provide informed consent. Patients will be excluded if they do not have an active mobile phone. The eligible participants will be allocated into intervention and control groups in a 1:1 ratio randomly. The intervention group will receive intervention of pre-designed text messages 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 receive text messages for 6 months as well as usual care. They will receive one general messages, one hypertension message, one glucose control message, one lifestyle message, one medication adherence message and one physical activity message per week. Outcome measures: The primary endpoint is the change in glycemic hemoglobin (HbA1C) as measured by central blood sample. Secondary endpoints include a change in proportion of patients achieving HbA1C<7%, body mass index (BMI), physical activity, medication adherence, systolic blood pressure, low-density lipoprotein cholesterol (LDL-C) and fasting blood glucose (FBG). Exploratory endpoints include long-term prognosis of the patients, such as death, nonfatal myocardial infarction, stroke and so on, as well as health status (SAQ and EQ-5D). 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, Diabetes
Keywords
Coronary artery disease, Diabetes, Text messages

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
502 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention-Text messaging
Arm Type
Experimental
Arm Description
Patients will receive regular semi-personalized text messages for 6 months. Each participants will receive 6 text messages per week, which will be sent at random times of the day (9.00am, 12noon, 4.00pm). They will receive one general messages, one hypertension message, one glucose control message, one lifestyle message, one medication adherence message and one physical activity message per week.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Participants in the control group will receive 2 thank-you messages per month and undertake routine clinical practice.
Intervention Type
Behavioral
Intervention Name(s)
Text messaging
Intervention Description
Patients will receive regular semi-personalized text messages for 6 months. Each participants will receive 6 text messages per week, which will be sent at random times of the day (9.00am, 12noon, 4.00pm). They will receive one general messages, one hypertension message, one glucose control message, one lifestyle message, one medication adherence message and one physical activity message per week. Prior to study commencement, a bank of 270 messages have been developed based on guidelines and behavior change theory (BCT), and have underwent multidisciplinary expert review and qualitative review process.
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
Change in proportion of patients achieving HbA1C<7%
Description
We will measure the change in proportion of patients achieving HbA1C<7% from baseline to 6 months.
Time Frame
Baseline; 6 months
Title
Change in level of fasting blood glucose (FBG)
Description
We will measure the change in FBG level from baseline to 6 months.
Time Frame
Baseline; 6 months
Title
Change in body mass index (BMI) according to national standards
Description
We will measured the change in BMI from baseline to 6 months.
Time Frame
Baseline; 6 months
Title
Change in systolic blood pressure (SBP) obtained in office during each interview
Description
We will measured the change in SBP from baseline to 6 months.
Time Frame
Baseline; 6 months
Title
Change in level of physical activity measured via International Physical Activity Questionnaire (IPAQ) scale
Description
We will measure the change in IPAQ scale from baseline to 6 months.
Time Frame
Baseline; 6 months
Title
Change in medication adherence
Description
We will measure the change in medication adherence from baseline to 6 months.
Time Frame
Baseline; 6 months
Title
Change in low-density lipoprotein cholesterol (LDL-C) level
Description
We will measure the change in LDL-C level from baseline to 6 months.
Time Frame
Baseline; 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participants with coronary artery disease defined as history of myocardial infarction and PCI History of diabetes Capability to read and send text messages Exclusion Criteria: Assumed poor adherence Do not have an active mobile phone
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lixin Jiang, MD, PhD
Organizational Affiliation
China National Center for Cardiovascular Disease
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Harlan M Krumholz, MD, SM
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fuwai hospital
City
Beijing
State/Province
Beijing
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
31474119
Citation
Huo X, Krumholz HM, Bai X, Spatz ES, Ding Q, Horak P, Zhao W, Gong Q, Zhang H, Yan X, Sun Y, Liu J, Wu X, Guan W, Wang X, Li J, Li X, Spertus JA, Masoudi FA, Zheng X. Effects of Mobile Text Messaging on Glycemic Control in Patients With Coronary Heart Disease and Diabetes Mellitus: A Randomized Clinical Trial. Circ Cardiovasc Qual Outcomes. 2019 Sep;12(9):e005805. doi: 10.1161/CIRCOUTCOMES.119.005805. Epub 2019 Aug 31.
Results Reference
derived
PubMed Identifier
29273661
Citation
Huo X, Spatz ES, Ding Q, Horak P, Zheng X, Masters C, Zhang H, Irwin ML, Yan X, Guan W, Li J, Li X, Spertus JA, Masoudi FA, Krumholz HM, Jiang L. Design and rationale of the Cardiovascular Health and Text Messaging (CHAT) Study and the CHAT-Diabetes Mellitus (CHAT-DM) Study: two randomised controlled trials of text messaging to improve secondary prevention for coronary heart disease and diabetes. BMJ Open. 2017 Dec 21;7(12):e018302. doi: 10.1136/bmjopen-2017-018302. Erratum In: BMJ Open. 2018 Jan 21;8(1):e018302corr1.
Results Reference
derived

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Cardiovascular Health and Text Messaging-Diabetes Mellitus (CHAT-DM) Study

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