Virtual visits after heart failure hospitalization: a lifeline or a gamble?
NCT ID NCT05724433
First seen Aug 07, 2026 · Last updated Aug 07, 2026
Summary
This trial tests whether a 3-month program of virtual visits and remote monitoring can improve recovery in adults recently hospitalized for heart failure. Participants receive either virtual heart failure care or routine care, and researchers track medication optimization, health status, and outcomes like death or readmission. The goal is to see if this digital approach can help patients get back on track and stay healthier.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Virtual heart failure care (virtual visits and remote monitoring)
- What this could lead to
- If effective, virtual care could become a standard way to help heart failure patients recover better after a hospital stay, potentially reducing deaths and readmissions.
- What could go wrong
- The trial is still testing this approach, and results may not show clear benefits. Virtual care may not suit all patients, and there are risks of technical issues or reduced personal interaction.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 891 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2023
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Adult patients ≥ 18 years old who: 1. Are being discharged after hospitalization or urgent visit for HF as 1. a primary diagnosis or 2. 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. 2. Have left ventricular ejection fraction (LVEF) \< 50% within the preceding 3 months. 3. Have NT-proBNP of \> 900 pg/ml during hospital admission or within 7 days after discharge from the ED 4. Have a mailing address for patient or caregiver 5. Provide verbal consent Exclusion Criteria: 1. Died or left hospital before medically advised hospital discharge 2. Unable to self-assess or communicate symptoms (e.g. clinically evident dementia) 3. Unable to engage with digital health technology or follow up 4. Severe valve disease 5. Recipient of or on waiting list for LVAD or cardiac transplant 6. Complex congenital heart disease, hypertrophic obstructive cardiomyopathy, or amyloid cardiomyopathy 7. 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 8. Severe kidney disease (persistent eGFR \< 30 mL/min/1.73m2) 9. Active malignancy 10. Receiving palliative care or expected life expectancy \< 6 months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
9 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Fattouma Bourguiba Hospital
RECRUITINGMonastir, Tunisia
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Hamilton General Hospital
RECRUITINGHamilton, Ontario, L8L 2X2, Canada
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Hedi Chaker Hospital
RECRUITINGSfax, Tunisia
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Juravinski Hospital Cancer Centre
RECRUITINGHamilton, Ontario, L8V 5C2, Canada
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Military Hospital
RECRUITINGTunis, Tunisia
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Sahloul Hospital
RECRUITINGSousse, Tunisia
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St. Joseph's Healthcare Hamilton
RECRUITINGHamilton, Onatrio, L8N 4A6, Canada
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Thunder Bay Regional Health Sciences Centre
NOT_YET_RECRUITINGThunder Bay, Ontario, Canada
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Unity Health Toronto
RECRUITINGToronto, Ontario, Canada
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Other studies related to the condition(s) this trial covers.
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- Can daily mindful breathing ease heart failure symptoms?
- Can a smartphone app keep heart failure patients out of the hospital?
- Can better training get doctors to talk about what matters most to dying veterans?
- Can AI read heart ultrasounds as well as trained sonographers?
- Can modern heart failure drugs reverse damage in three months?