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NCT07720349Recruiting

Digital Long-term Follow-up of Patients With Coronary Artery Disease

Digital Long-term Follow-up of Patients With Coronary Artery Disease: a Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 31 Jul 2026

Brief summary (registry, in English)

The need for better follow-up of AMI patients combined with recent developments in the digital area prompted the Department of Cardiology (HJE) at Oslo University Hospital (OUS) Ullevål, in collaboration with the Department of Digital Health Research (DIG) at OUS to develop a digital solution for long-term follow-up after AMI. The overall goal of the digital solution is to increase knowledge and awareness about important lifestyle measures and CV risk factors in patients who have survived an AMI, and to make it easy for the patients to monitor their own risk factors and attainment of treatment goals during long-term follow-up. Further, the HeartCheck seeks to provide guidance to ensure medication adherence. In this project, we study whether this newly developed app (HeartCheck), through education, regular reminders and easily understandable goals for secondary prevention, can improve risk factor control and drug adherence during long-term follow-up after AMI. A randomized controlled trial (RCT) is the chosen study design, being the gold standard for testing effectiveness of interventions.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
630 (estimated)
First submitted
17 Jul 2026
Start date
1 Apr 2026
Primary completion date
31 Dec 2028
Lead sponsor
Oslo University Hospital
NCT number
NCT07720349

What you commit to

  • Study type: Interventional
  • Planned participants: 630
  • From 1 Apr 2026 to the primary completion date, 31 Dec 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • patient is unable to comply with the study procedures due to severe comorbidities or high age

Other

  • patient does not understand Norwegian

Who the study is looking for

  • \>18 years of age
  • survived a recent (\<30 days) AMI and/or PCI
  • access to a smartphone or tablet
  • signed written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sørlandet hospital Arendal
Coordinator of this site? Confirm its status
ArendalNorwayRecruiting
Oslo University Hospital Ullevål
Coordinator of this site? Confirm its status
OsloNorwayRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.