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Prospective exploration of the effect of transitional care based on telemonitoring on the prognosis of patients with chronic heart failure

Prospective exploration of the effect of transitional care based on telemonitoring on the prognosis of patients with chronic heart failure

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061940
Enrollment
Unknown
Registered
2022-07-11
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

heart failure

Interventions

Group 1 :Outpatient review
Group 2:Telemonitoring

Sponsors

PLA General Hospital Medical Big Data Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Hospitalization due to the primary or secondary diagnosis of heart failure (defined according to the International Classification of Diseases code (ICD-10)) in the last 12 months; 2. According to the echocardiographic examination in the last 12 months, the left ventricular ejection fraction (LVEF) is = 18 years old; 5. Receive at least one heart failure drug treatment (such as diuretics); 6. Own a smartphone.

Exclusion criteria

Exclusion criteria: 1. Hospitalization within 14 days before randomization; 2. Have implantable heart assist devices (pacemaker, artificial valve, etc.); 3. Acute coronary syndrome within 14 days before randomization; 4. Planned coronary revascularization, transcatheter aortic valve implantation (TAVI), cardiac resynchronization therapy (CRT) and/or heart transplantation (HTX) within 28 days before randomization or within 3 months after randomization; 5. End-stage heart failure (hospice candidates with limited life expectancy); 6. End-stage renal disease (stage IV, glomerular filtration rate < 30 ml/min, or hemodialysis); 7. Pulmonary heart disease; 8. Active cancer; 9. Alcohol or drug abuse; 10. Pregnancy; 11. Unable or unwilling to use remote monitoring equipment (such as unable to take care of themselves, dementia, lack of communication skills); 12. Will be or have been living in a nursing home or other nursing facility after discharge from the hospital; 13. Depression, cognitive impairment, etc.; 14. Have been or are currently participating in similar trials.

Design outcomes

Primary

MeasureTime frame
The percentage of days lost due to unplanned cardiovascular hospitalisations or all-cause death;

Secondary

MeasureTime frame
All-cause readmission and/or death;Readmission and/or death due to heart failure;Heart failure-related quality of life score;Health care costs;

Countries

China

Contacts

Public ContactHe Kunlun

PLA General Hospital Medical Big Data Center

kunlunhe301@gmail.com+86 13911232619

Outcome results

None listed

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