About this trial
The goal of this observational study is to evaluate the implementation of a structured, digital, nurse-led, remote monitoring care pathway for cardiovascular risk management (CVRM). Participants will receive this care as part of routine clinical practice. In addition to standard follow-up, participants will complete questionnaires on quality of life, medication adherence, system usability, and patient satisfaction.
Eligibility criteria
Qualifiers
Age ≥18 years
All patients enrolled in the program (high-risk and very high-risk patients)
Disqualifiers
Not able to provide informed consent
No access to smartphone and/or tablet
Inability to use digital tools required for the program
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Lead sponsor
Cardiology Centres of the Netherlands
Collaborator