Secondary Prevention With the Lifestyle Tool
Condition(s) studied
Investigational drug(s) / intervention(s)
Lifestyle tool: Regular use of the digital Lifestyle tool
Study summary
In this study participants will be randomized to use a digital lifestyle tool over three years or to a control group without access to the tool. The investigators will prospectively follow the incidence of major cardiovascular events in patients who have previously suffered from a myocardial infarction in those using the tool regularly and those in the control group.
Eligibility
Primary outcome measure(s)
- Incidence of major adverse cardiovascular event — 3 years
Incidence of major adverse cardiovascular event, defined as cardiovascular death, myocardial infarction, stroke, or hospitalization for heart failure compared between participants regularly using the tool and on usual care.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Skane University Hospital | Malmö | Sweden | Recruiting |
More Region Skane trials in Sweden
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05309876 on ClinicalTrials.gov ↗ ← All trials in Sweden