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Clinical study of APP-assisted individualized self-management for patients with atrial fibrillation

Clinical study of APP-assisted individualized self-management for patients with atrial fibrillation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106502
Enrollment
Unknown
Registered
2025-07-24
Start date
2023-02-14
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

atrial fibrillation

Interventions

Research Group:APP Management

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age>=18 years old, =2 points for men and >=3 points for women 4. The patient or a relative who has lived with him for a long time is using a smartphone

Exclusion criteria

Exclusion criteria: 1. Presence of moderate to severe valvular disease 2. Presence of congenital heart disease 3. Planned to receive atrial fibrillation catheter ablation or left atrial appendage occlusion treatment in the near future 4. Severe heart failure (cardiac function class VI, and/or EF <35%) and severe organic heart disease 5. Contraindications to anticoagulant therapy 6. Pregnant women 7. Have had or plan to undergo major surgical procedures in the near future 8. Estimated life expectancy < 12 months 9. Unable to communicate normally due to mental or intellectual disability, or hearing or language impairment 10. Unable to sign informed consent or refuse to participate in the study

Design outcomes

Primary

MeasureTime frame
Anticoagulant use rate at 12 months;

Secondary

MeasureTime frame
Other guideline recommended drug utilization rates;Number of emergency room visits and hospitalizations related to atrial fibrillation within 12 months;Number of nurse/doctor phone contacts;

Countries

China

Contacts

Public ContactBing Han

Xuzhou Central Hospital

Hbing777@hotmail.com+86 135 0521 8127

Outcome results

None listed

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