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Digital Remote Management for Care and Continuous Optimization Versus Usual Care for Optimization of Guideline-directed Medical Therapy in Patients With Heart Failure and Reduced Ejection Fraction (DigiCare-HFrEF): a Multicentre, Randomised, Controlled Trial

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

DigiCare-HFrEF is an investigator-initiated, multicentre, randomised, open-label, endpoint-blinded, superiority trial designed to evaluate whether a structured digital remote-management platform can optimise guideline-directed medical therapy (GDMT) in patients with heart failure with reduced ejection fraction (HFrEF) after hospital discharge. Eligible adults (≥18 years) with a confirmed diagnosis of HFrEF within the past 3 months (left ventricular ejection fraction ≤40%) who are not optimally treated with GDMT-defined as at least two of the four foundational drug classes (ACEi/ARB or ARNi, β-blocker, MRA, SGLT2 inhibitor) either not initiated or prescribed at \<50% of the target dose-will be randomly assigned in a 1:1 ratio to digital remote management or usual care. In the intervention arm, patients will report symptoms and key physiologic measures (e.g., blood pressure, heart rate, and body weight) via the platform; an algorithm will perform risk stratification and generate GDMT optimisation suggestions and decongestion prompts, as well as a comprehensive management for core health metrics, which are reviewed and confirmed by clinicians before implementation. The primary endpoint is the change in GDMT score from baseline to 3 months (ΔGDMT).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adults aged ≥18 years.

• Hospitalised at a secondary or tertiary hospital with established heart failure care capacity.

• Diagnosed with HFrEF within the past 3 months according to the 2022 ACC/AHA/HFSA guideline diagnostic pathway, including: LVEF ≤40% by echocardiography; typical heart-failure symptoms and/or signs; and exclusion of non-HF causes of symptoms.

• Not optimized on guideline-directed medical therapy (GDMT) at enrollment, defined as at least two of the following four foundational drug classes not initiated or administered at \<50% target dose.

• Written informed consent provided.

Locations
Other Locations
China
Beijing Anzhen Hospital, Capital Medical University, Beijing, China
RECRUITING
Beijing
Beijing Tongren Hospital, Capital Medical University, Beijing, China
RECRUITING
Beijing
The First Affiliated Hospital of Dalian Medical University, Dalian, China
RECRUITING
Dalian
The First Hospital of Jilin University, Changchun, China
RECRUITING
Jilin City
The Second Affiliated Hospital of Nanchang University, Nanchang, China
NOT_YET_RECRUITING
Nanchang
Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
NOT_YET_RECRUITING
Shanghai
Contact Information
Primary
DigiCare-HFrEF Coordinating Center
chshma@vip.sina.com
chshma@vip.sina.com
Time Frame
Start Date: 2026-02-26
Estimated Completion Date: 2026-07
Participants
Target number of participants: 252
Treatments
No_intervention: Usual Care
Usual Care with guideline-recommended outpatient follow-up. No platform-based risk stratification or decision support is provided.
Experimental: Digital Remote Management
Participants will use a digital remote-management platform to report symptoms and key physiologic variables (e.g., blood pressure and body weight). The platform applies a predefined risk-stratification algorithm and provides clinician-facing decision support for GDMT titration and congestion management. A comprehensive management for core health metrics will also be provided. Clinicians review and confirm recommendations before they are communicated to patients.
Related Therapeutic Areas
Sponsors
Leads: Beijing Anzhen Hospital
Collaborators: The First Hospital of Jilin University, Second Affiliated Hospital of Nanchang University

This content was sourced from clinicaltrials.gov