NCT05972746

Telemonitoring Program in the Vulnerable Phase After Hospitalization for Heart Failure

Telemonitoring Program With Electronic Alerts to Improve Outcomes in the Vulnerable Phase After Hospitalization for Heart Failure: A Pragmatic Clinical Trial TREAT - Vulnerable HF

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 110 (estimated)
• Sponsor: Instituto Cardiovascular de Buenos Aires · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This pragmatic clinical trial aims to evaluate the impact of a telemonitoring program with an electronic alert system compared to standard treatment on the perception of self-care in patients after hospitalization for decompensated HF at 3 months post-discharge. And secondarily to evaluate its impact on clinical events, NT-proBNP and efficacy and safety to facilitate the use and titration of the recommended drugs in patients with reduced ejection fraction at 90 days.

Conditions

• Heart Failure
• Acute Heart Failure

Interventions

Type	Name	Description
DEVICE	Telemonitoring with electronic alerts	Patients assigned to this group will receive standard care plus a telemonitoring program.
OTHER	Standard of care	Standard of care

Timeline

• Start date: 2022-10-07
• Primary completion: 2023-10-07
• Completion: 2023-11-07
• First posted: 2023-08-02
• Last updated: 2023-08-02

Locations

1 site across 1 country: Argentina