Peer-led Digital Health Lifestyle Intervention for a Low Income Community at Risk for Cardiovascular Diseases (MYCardio-PEER)

Monash University Malaysia

Status: Completed

Conditions: Primary Prevention of Cardiovascular Diseases

Treatments: Behavioral: MYCardio-PEER

Study type: Interventional

Funder types: Other

Identifiers

NCT06408493

36440

Details and patient eligibility

About

The goal of this interventional study is to develop and assess the effectiveness of a peer-led digital health program (MYCardio-PEER) for primary prevention of cardiovascular disease (CVD) in a low-income community at-risk of CVD.

The main questions it aims to answer are:

• Is MYCardio-PEER effective in improving knowledge, lifestyle behaviors and CVD biomarkers of a low-income community at-risk for CVD?
• Is there an association between MYCardio-PEER participants' adherence and satisfaction, with effectiveness and sustainability of the program?

Participants will attend the 8-weeks MYCardio-PEER program with their peer leaders, supplemented with face-to-face components. Participants will then be followed up for another 12 weeks, during which peer leaders and researchers will have minimal contact with the participants. Participants who have been allocated into the control group will receive printed documents with standard tips on dietary and lifestyle management for CVD, where they will be encouraged to maintain regular calorie intake and expenditure and perform regular exercise.

Enrollment: 63 patients

Sex: All

Ages: 30 to 74 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Mentally sound man/woman of at least 30 years old
• Monthly household income of less than RM3,710 or receiving government aid for low-income community
• Literate with a fair command of the Malay language
• Have mobile device connected to the Internet
• Willing to attend 8 weeks of intervention and be followed up for another 12 weeks during the maintenance phase.
• Have been confirmed to have a moderate or high risk for CVD based on the Framingham General CVD Risk Score

Exclusion criteria

• Pregnant, lactating or intend to become pregnant during the study period.
• Any other pre-existing conditions or severe complications that could compromise the ability to adhere to the study program.
• Enrolled in other studies.

Trial design

Primary purpose: Prevention

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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63 participants in 2 patient groups

Intervention

Experimental group

Description:

Participants will attend the 8-weeks MYCardio-PEER program with their peer leaders, supplemented with face-to-face components.

Treatment:

Behavioral: MYCardio-PEER

Control

No Intervention group

Description:

Participants will receive printed documents with standard tips on dietary and lifestyle management for CVD.