VIrtual Care To Improve Outcomes and RecoverY From Heart Failure Hospitalization
Recruiting now NCT05724433
Run by Population Health Research Institute · for 18 and older · All sexes
What this study is about
The clinic visits (intervention) will continue for 90 days, which represents the follow-up period for the primary medication and health status outcomes. The co-primary clinical outcomes will be obtained at 180 days.
Who can join (things the study team will check)
✅ You may be able to join if…
- Are being discharged after hospitalization or urgent visit for HF as
- a primary diagnosis or
- significant complication (prolonging length of stay) of another diagnosis OR Have been referred for an initial consult at a cardiology clinic within 1 week of hospitalization or urgent visit for HF as a primary or secondary diagnosis, as described above.
- Have left ventricular ejection fraction (LVEF) < 50% within the preceding 3 months.
- Have NT-proBNP of > 900 pg/ml during hospital admission or within 7 days after discharge from the ED
- Have a mailing address for patient or caregiver
- Provide verbal consent
🚫 You may not be able to join if…
- Died or left hospital before medically advised hospital discharge
- Unable to self-assess or communicate symptoms (e.g. clinically evident dementia)
- Unable to engage with digital health technology or follow up
- Severe valve disease
- Recipient of or on waiting list for LVAD or cardiac transplant
- Complex congenital heart disease, hypertrophic obstructive cardiomyopathy, or amyloid cardiomyopathy
- Severe lung disease with symptoms on minimal exertion, forced expiratory volume during 1 second (FEV1) < 1 litre, severe pulmonary hypertension with RVSP > 60 mm Hg, or on home oxygen
- Severe kidney disease (persistent eGFR < 30 mL/min/1.73m2)
- Active malignancy
- Receiving palliative care or expected life expectancy < 6 months
Where this trial is running
- St. Joseph's Healthcare Hamilton, Hamilton, Onatrio, Canada
- Hamilton General Hospital, Hamilton, Ontario, Canada
- Juravinski Hospital Cancer Centre, Hamilton, Ontario, Canada
- Thunder Bay Regional Health Sciences Centre, Thunder Bay, Ontario, Canada
- Unity Health Toronto, Toronto, Ontario, Canada
- Fattouma Bourguiba Hospital, Monastir, Tunisia
- Hedi Chaker Hospital, Sfax, Tunisia
- Sahloul Hospital, Sousse, Tunisia
- Military Hospital, Tunis, Tunisia
Who to contact
Harriette GC Van Spall, MD MPH · (905) 521-2100 · Harriette.VanSpall@phri.ca
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT05724433.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.
Beacon is an information tool, not medical advice. Whether a trial is right for you is a decision for you, your doctor, and the study team. Trial details come from the official registry, ClinicalTrials.gov, and may change — always confirm with the study team. Beacon collects no data about you: this page has no cookies, no accounts, and no tracking.