Comprehensive Management of High-risk PopuLatIon of Stroke Based on Social Network (COMPLIANCE-MT)

Naval Military Medical University

Status: Enrolling

Conditions: Stroke; Central Nervous System Diseases; Cardiovascular Diseases; Nervous System Diseases; Vascular Diseases; Cerebrovascular Disorders; Brain Diseases

Treatments: Behavioral: Post-hospital management based on WeChat applet; Behavioral: Routine post-hospital follow-up management

Study type: Interventional

Funder types: Other

Identifiers

NCT05963828

COMPLIANCE-MT

Details and patient eligibility

About

The purpose of this study is to evaluate the effectiveness of social network in improving drug compliance and risk factors control rate of stroke high-risk population after discharge.

Full description

Stroke is the leading cause of death among residents in China, with the characteristics of high morbidity, high mortality, high disability rate, high recurrence rate and so on, which brings huge economic burden to the patients' families and society. Strengthening the comprehensive management of the high-risk population of stroke, improving the medication compliance of patients and the control rate of stroke risk factors play a key role in reducing stroke recurrence.

This study is a multicenter, prospective, randomized, single-blind study, which aims to use the tool of WeChat Mini Programs to realize the post-hospital follow-up management of the high-risk population of stroke. The follow-up time is 12 months. The main measurement result was the change of patients' medication compliance after comprehensive management.

Enrollment: 720 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age ≥18 years
• High-risk population of stroke for hospitalization
• Modified Rankin Scale score≤ 2
• Patients or primary caregiver have smart phone and wechat accounts
• Patients take at least one drug for a long time (antihypertensive, hypoglycemic, lipid-lowering, anticoagulant, antiplatelet drugs)
• Written informed consent

Exclusion criteria

• Patients and their families are unable to operate smartphones
• Having other diseases that interfere with clinical follow-up assessment (such as cancer, dementia, severe mental illness, etc.)
• Life expectancy is less than 12 months
• Patients living in the absence of network conditions

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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720 participants in 2 patient groups

Standard group

Other group

Description:

Patients are managed according to the routine methods after enrollment.

Treatment:

Behavioral: Routine post-hospital follow-up management

Experimental group

Experimental group

Description:

Patients are managed by the social network platform.

Treatment:

Behavioral: Post-hospital management based on WeChat applet