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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04192409
Acronym
GUIDEME
Enrollment
1038
Registered
2019-12-10
Start date
2020-01-01
Completion date
2022-06-30
Last updated
2023-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Bypass, Coronary Artery Disease, Diabetes Mellitus

Keywords

Coronary Artery Disease, Coronary Artery Bypass Grafting, Diabetes Mellitus, Smartphone Application, Postoperative Management

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.

Interventions

BEHAVIORALSmartphone Application

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.

Sponsors

Chinese Academy of Medical Sciences, Fuwai Hospital
CollaboratorOTHER
China National Center for Cardiovascular Diseases
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in glucose level measured by HbA1C levelBaseline; 6 monthsWe will measured the change in glucose level from baseline to 6 months.

Secondary

MeasureTime frameDescription
The incidence of major adverse cardiovascular events(MACE)6 monthsWe will measure the incidence of major adverse cardiovascular events(MACE) at 6 months.
EQ-5D6 monthsWe will measure the change in EQ-5D health survey 6 months postoperatively.
Medication adherence6 monthsMedication 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.
The incidence of all-cause death6 monthsWe will measure the incidence of all-cause death at 6 months.
blood pressure6 monthsWe will document blood pressure at 6 months postoperatively.
blood glucose6 monthsWe will document blood glucose at 6 months postoperatively.
low density lipoprotein6 monthsWe will document low density lipoprotein at 6 months postoperatively.
Status of the graft vessels6 monthsWe will measure the status of the graft vessels by coronary CT angiography at 6 months.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026