Ireland
--:--IST
Recruiting Not applicable

Secondary Prevention With the Lifestyle Tool

NCT05309876 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2022-04-06
Last updated
2025-07-16

Condition(s) studied

Cardiovascular Diseases

Investigational drug(s) / intervention(s)

Lifestyle tool

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

Sex
ALL
Min age
35 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * age 35 to 80 years * myocardial infarction within one year prior to enrolment * access to computer or mobile phone. Exclusion Criteria: * conditions or treatments that in the judgement of the Investigator could affect the study evaluation

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)

FacilityCityRegionStatus
Skane University Hospital Malmö Sweden Recruiting
Official registry record

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