Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Heart@Home: Safe, at-home care for people with acute heart problems compared with hospital care

Official title: Heart@Home Safety and Efficacy of Hospital-at-Home Care Versus Standard Hospitalization in Cardiac Patients

Run by Tel-Aviv Sourasky Medical Center · NCT07913152 · Data updated 2026-11-12

This trial tests whether hospital-level care at home can safely and effectively treat adults with acute heart conditions who would normally be in the hospital.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment150 (estimated)
SponsorTel-Aviv Sourasky Medical Center
Government
Locations1 site (Tel Aviv)
StatusRecruiting
StartedJune 17, 2026
Main results expectedNovember 30, 2027
Study endsDecember 31, 2027
Registry record updatedNovember 3, 2026
Trial IDNCT07913152 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18) with an acute cardiovascular condition who are clinically stable, live in the Tel Aviv area, have Wi‑Fi and caregiver support for initial 24 hours, and can use the required technology.

Probably not a fit

Patients unable to meet stability, home environment, or technological requirements, or those at high risk of rapid deterioration, may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

In this prospective randomized trial, adults with acute cardiovascular conditions are assigned to Hospital-at-Home care or standard in-hospital care to see if remote monitoring at home provides similar safety and benefits. The study enrolls about 150 participants from Tel Aviv Sourasky Medical Center who have conditions such as acute myocardial infarction, pericarditis, myocarditis, pulmonary embolism, heart failure, or post-procedural cardiac interventions. Remote cardiovascular monitoring and support at home are used to manage therapy, vital signs, and potential complications. Outcomes of safety, efficacy, and healthcare utilization will be compared between groups.

Why it matters

Potential benefit: If successful, patients may experience hospital-level care at home with comparable safety, potential reduced length of stay, and greater comfort.

How similar studies have gone: Prior hospital-at-home programs in other medical areas have shown feasibility, with mixed results; this trial adds cardiovascular-specific data.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥18 years.
* Residence in the Tel Aviv area, allowing accessibility of the treating team and a rapid response when required.
* Mental capacity to provide informed consent and the ability to understand and follow medical recommendations.
* Availability of a family member or caregiver who agrees to remain with the patient during the first 24 hours of Hospital-at-Home care and to be available for periodic assessments as needed. This requirement may be waived at the discretion of the patient and treating physician for highly independent patients.
* Suitable home environment with Wi-Fi connectivity to support remote monitoring.
* Adequate technological literacy of the patient or caregiver to use the required technology.
* Clinically stable and at low risk of rapid deterioration, based on vital signs and initial assessments as determined by the treating physician.
* The primary indication for hospitalization is one of the following: acute myocardial infarction, pulmonary embolism, pericarditis/myocarditis, heart failure, following transcatheter valve replacement or repair, following pacemaker or implantable cardioverter-defibrillator implantation,.

Disease-Specific Inclusion Criteria

In addition to the general inclusion criteria, patients must meet the relevant disease-specific criteria:

1. Acute Myocardial Infarction

   Acute myocardial infarction with or without ST-segment elevation (STEMI or NSTEMI), treated with primary percutaneous coronary intervention (PCI). The intervention must have been performed in a coronary artery other than the proximal left anterior descending (LAD) artery or left main coronary artery, with TIMI grade III flow at the end of the procedure, no additional critical coronary artery stenoses, an uncomplicated PCI without periprocedural complications, and preserved left ventricular systolic function (LVEF \>45%).
2. Pericarditis/Myocarditis

   Initial diagnosis of pericarditis or myocarditis, with no more than a mild pericardial effusion and preserved left ventricular systolic function (LVEF ≥50%).
3. Pulmonary Embolism

   Low-intermediate-risk pulmonary embolism following echocardiographic and CT angiographic (CTA) assessment and treatment with oral or subcutaneous anticoagulation; or intermediate-high-risk pulmonary embolism following successful mechanical thrombectomy, with subsequent improvement in hemodynamic and echocardiographic parameters.
4. Following Transcatheter Valve Replacement or Repair

   Patients following uncomplicated transcatheter aortic valve replacement (TAVR), or transcatheter edge-to-edge repair (TEER) of the mitral or tricuspid valve, with no clear indication for pacemaker implantation.
5. Heart Failure

   Newly diagnosed (de novo) heart failure or worsening of pre-existing heart failure, regardless of left ventricular ejection fraction (LVEF), with symptomatic NYHA functional class II-IV heart failure requiring hospitalization.
6. Following Pacemaker or Implantable Cardioverter-Defibrillator Implantation.

Exclusion Criteria:

* Pregnancy.
* Inability to provide informed consent.
* Clinically unstable medical condition or significant risk of developing hemodynamic or cardiovascular instability.
* Requirement for continuous intravenous infusion of fluids or medications.
* Uncontrolled pain.
* Active significant non-cardiovascular comorbid condition, including acute ischemic stroke, active bleeding, severe exacerbation of pulmonary disease, or sepsis.
* Hemoglobin \<8 g/dL.
* Estimated glomerular filtration rate (eGFR) \<20 mL/min/1.73 m².
* History of non-adherence to medical treatment or failure to attend follow-up visits.
* Residence in a facility that provides on-site medical care, such as a nursing facility.
* Significant cognitive impairment interfering with the patient's ability to adhere to treatment or participate in education and self-care.
* Inability to obtain peripheral intravenous access, including vascular access requiring ultrasound guidance.

Where it's running

  • Tel Aviv Sourasky Medical Center
    Tel Aviv, Israel
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.