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Integrating CardioCare: Advancing post-screening cardiovascular management in health check-up centers

Integrating CardioCare: Advancing post-screening cardiovascular management in health check-up centers

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103369
Enrollment
Unknown
Registered
2025-05-28
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Cardiovascular disease

Interventions

Intervention group:Participants in the intervention group will receive personalized messages from the CardioCare system on a weekly basis. These messages will include feedback and reminders concerning
Control group:During the 12-month study, participants in the control group will receive standard care, including health check-up results notification and recommendations to visit outpatient clinics fo

Sponsors

Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria includes participants: 1. who are 50 years or older; 2. with a calculated 10-year CVD risk exceeding 10% using an established risk score based on the Guangzhou Biobank Cohort Study (GBCS) model; 3. provide written informed consent to participate; 4. have access to a mobile phone or a device capable of receiving messages and feedback from the CardioCare system.

Exclusion criteria

Exclusion criteria: Exclusion criteria includes participants: 1. with previously diagnosed cardiovascular disease; 2. with severe comorbid conditions that would prevent them from participating in regular follow-up assessments or adhering to the study protocol (e.g., advanced cancer, severe cognitive impairment); 3. with a life expectancy of less than one year, as determined by their healthcare provider; 4. who do not reside in Guangzhou and are unlikely to remain in the area for the duration of the study; 5. who have previously participated in similar CVD management programs or studies that might influence the outcomes of the current study.

Design outcomes

Primary

MeasureTime frame
Recruitment rate;Participant retention;Adherence to the intervention protocol;

Secondary

MeasureTime frame
Estimated 10-year CVD risk;Adherence to medication;Lifestyle modification;Patient engagement with the CardioCare System;Usability and satisfaction of the CardioCare System;

Countries

China

Contacts

Public ContactLin Xu

Sun Yat-sen University

xulin27@mail.sysu.edu.cn+86 20 8733 5523

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026