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Mobile Health (mHealth) technology for improved screening, patient involvement and optimizing integrated care in atrial fibrillation

Mobile Health (mHealth) technology for improved screening, patient involvement and optimizing integrated care in atrial fibrillation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-OOC-17014138
Enrollment
Unknown
Registered
2017-12-26
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-12-10

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

Conditions

Atrial fibrillation

Interventions

atrial fibrillation population:AF screening and integrated ABC strategy

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. patients aged = 18 years old, diagnosed with new-onset, paroxysmal, persistent or permanent atrial fibrillation with electrocardiogram (ECG), 24 hour Holter monitors; 2. CHA2DS2-VASc score = 2.

Exclusion criteria

Exclusion criteria: Those with mechanical prosthetic valve AF or moderate/severe mitral stenosis, unable to provide informed consent, unable to have one year of follow-up for any reason.

Design outcomes

Primary

MeasureTime frame
Composite endpoint of stroke/thromboembolism, death, and rehospitalization;

Secondary

MeasureTime frame
change in proportion of patients able to continue anticoagulation;MAFA intervention costs, individual-level HealthCare Resource Utilization (HCRU) as well as associated costs, and quality adjusted life year (QALY) gained with MAFA compared to usual care;Identified AF rate;

Countries

China

Contacts

Public ContactChen Yundai

Chinese PLA General Hospital

Yundai_Chen301@163.com+86 010 55499209

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 2, 2026