Evaluation of a mobile app for cardiac patient follow-up

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This trial evaluates a mobile application designed to support patients with atrial fibrillation and heart failure in managing their conditions at home. The app provides educational resources, allows users to track health metrics, manage medications, and assess their quality of life through questionnaires. The study focuses on assessing the app's usability, long-term adherence, and patient satisfaction over time. By leveraging technology, the trial aims to enhance patient engagement and improve health outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Age ≥ 18 years,
2. Patients in whom AF or atrial flutter is diagnosed with an electrocardiogram (12-lead, Holter monitor,…) and/or patients in whom HF is diagnosed in their medical records,
3. Patients who are capable of signing the informed consent.

Exclusion Criteria:

1. Not able to speak and read Dutch,
2. Cognitive impaired (e.g. severe dementia),
3. No smartphone or tablet available.

Where it's running

• University Hospital Antwerp
  Edegem, Antwerp, Belgium Recruiting

Study contacts

• Principal investigator: Hein Heidbuchel — University Hospital, Antwerp
• Study coordinator: Lieselotte Knaepen
• Email: lieselotte.knaepen@uhasselt.be
• Phone: 003238213947

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.