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Research on the life-cycle comprehensive prevention and control of cardiovascular diseases (hypertension-atrial fibrillation-stroke) and information technology support in primary care (HAS study)

Research on the life-cycle comprehensive prevention and control of cardiovascular diseases (hypertension-atrial fibrillation-stroke) and information technology support in primary care (HAS study)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300076331
Enrollment
Unknown
Registered
2023-10-04
Start date
2023-10-10
Completion date
Unknown
Last updated
2023-10-09

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

Conditions

Hypertension, Atrial fibrillation, Stroke

Interventions

People at high risk of atrial fibrillation:Wearable ECG screening and whole process management based on digital platform.
Patients with atrial fibrillation:Whole process management based on digital platform.
Patients with Stroke:Whole process management based on digital platform.

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: This cohort consisted of three subcohorts, including subcohorts of people at high risk of atrial fibrillation (hypertension and et.al) , atrial fibrillation and stroke, which are not independent. 1. Cohort of people at high risk of atrial fibrillation: (1) Patients with hypertension in rural areas or communities; (2) At least 18 years old; (3) Wear wearable ECG devices voluntarily; (4)Voluntary participation in the whole process management based on the information platform. 2. Atrial Fibrillation cohort: (1) Patients from cohort of people at high risk of atrial fibrillation; (2) Diagnosis of atrial fibrillation by ECG; (3) Voluntary participation in the whole process management based on the information platform. 3. Stroke cohort (1) Source atrial fibrillation cohort; (2) Diagnosed stroke (3) Voluntary participation in the whole process management based on the information platform.

Exclusion criteria

Exclusion criteria: 1. Atrial fibrillation screening cohort: (1) Patients with cardiac pacemaker or ICD; (2) A history of severe skin allergy; (3) Refuse to sign informed consent. 2. Atrial Fibrillation cohort: (1) Mentally ill or cognitively impaired, unable to express themselves correctly; (2) Refuse to sign informed consent. 3.Stroke cohort (1) Mentally ill or cognitively impaired, unable to express themselves correctly; (2) Refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Major adverse cardiovascular events(MACE) ,including cardiac death, nonfatal myocardial infarction, heart failure, nonfatal stroke.;

Secondary

MeasureTime frame
Detection rate of atrial fibrillation;Anticoagulation rate of atrial fibrillation;Compliance with treatment;systemic thromboembolic events;all-cause death;cardiovascular disease hospitalization events;Assessment of quality of life.;

Countries

China

Contacts

Public ContactXiaoyang Liao

West China Hospital, Sichuan Universit

liaoxiaoyang@wchscu.cn+86 28 8542 1246

Outcome results

None listed

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