Can a smartphone app keep heart attack patients out of the ER?
NCT ID NCT07171580
First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tests whether digital health tools can help people recover safely at home after a heart attack. Researchers will compare two types of follow-up care: education alone versus education plus extra support like symptom tracking and virtual appointments. The goal is to reduce emergency visits and improve mental well-being for 300 patients in Manitoba.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- digital health platform (remote education and support)
- What this could lead to
- If successful, this could create a better support system for heart attack survivors, reducing hospital visits and improving recovery, especially for rural patients.
- What could go wrong
- This is an early-stage study with 300 participants, so results may not apply to everyone. Technology barriers or lack of engagement could limit its effectiveness.
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 300 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2025
An estimate. Start dates often move.
- Expected to finish
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Apr 2027
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: \>18 years old, type 1 myocardial infarction27, resident of Manitoba Exclusion Criteria: Patients unable to consent or fully participate in the study due to: 1. Technology barriers 1. Lack of digital device, internet access or data 2. Discomfort with using technology 2. Communication or language barriers preventing participation 3. Cognitive or mental health limiting informed consent or participation 1. Dementia or cognitive impairment 2. Active or severe psychosis or other significant mental health conditions c. Active substance abuse 4. High-risk ACS where patients require more frequent or in person visits a. Cardiac: i. Coronary * Unrevascularizedleftmainormultivessellargeepicardialcoronary artery disease (\>2.5mm) * Coronary artery bypass surgery (CABG) during index hospitalization ii. Arrhythmias * Cardiac arrest during index event/hospitalization (ventricular tachycardia (VT)/ventricular fibrillation (VF), pulseless electrical activity (PEA)) iii. Cardiomyopathy * Left ventricular ejection fraction (LVEF) \<35% (most recent EF assessment) * Cardiogenic shock requiring pressors/inotropes for more than 24 hours * Requiring intubation/positive pressure ventilation/hi-flow oxygen for more than 24 hours * Switchedfromintravenous(IV)tooral(PO)loopdiureticwithinlast 48 hours * Change in PO loop diuretic dose within last 48 homes (home re- start of 80mg or less is allowed) * B-type natriuretic peptide (BNP) did not reduce by 30% iv. Cardiac Care Unit (CCU)/Intensive Care Unit (ICU) o Any CCU/ICU stay for more than 24 hours b. Medical: i. any condition with prognosis less than 1 year or a high LACE (Length of stay, Acuity of admission, Comorbidities, Emergency department use) score (\>15)28 ii. any medical comorbidity requiring in-person assessment within 2 weeks TPD-REACH PROTOCOL v3 29Aug2025 8 of 17 TPD-REACH: Remote Education and Access for Cardiac Health iii. transition to an alternative living arrangement/compromised independent living iv. need medication adjustment or investigation within 2 weeks c. Social: i. severe financial strain ii. no fixed address or housing instability iii. severe food insecurity iv. significant hearing or vision impairment v. poor health literacy While we aim to promote health equity, patients facing these challenges need more support than this project can offer and should be connected to appropriate services before discharge. 5. Non-atherosclerotic causes of ACS (spontaneous coronary artery dissection, stress- induced cardiomyopathy, myocarditis) as the education and treatment is different 6. Any additional factor preventing full participation in the study
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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
1 site. 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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St Boniface Hospital
Winnipeg, Manitoba, R2H 2A6, Canada
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Every minute counts: study tracks how delays shape heart attack survival
- The heart rhythm threat hiding in heart attack wards
- Tailoring cardiac rehab to each heart: can personalized training speed recovery?
- Can a 20-Minute playlist calm a heart attack Patient's nerves?
- Heart pump timing put to the test in deadly heart attack shock
- AI on your phone: the future of heart attack detection in the field?