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NCT06869408Completed

Observational Study on the Patient's Ability to Use a Digital Platform in Heart Failure

Source: ClinicalTrials.gov · Last updated 31 Jul 2025

Brief summary (registry, in English)

Heart Failure has a global prevalence of 1 to 3% in the adult population with an incidence of 1 to 20 cases per 1,000 people. Furthermore, HF is often associated with a number of comorbidities (anaemia, arrhythmias, depression, hyperuricemia, coronary heart disease etc.), which greatly deteriorates the patient's quality of life. Despite the development of specific drugs, HF has a very high mortality rate, and it is the first cause of unscheduled income. An increase of 50% of these incomes is expected in the next 25 years. In this context, the use of digital tools/platforms that allow remote monitoring of patients and that facilitate telemedicine have shown potential to improve treatment adherence and facilitate continued therapeutic education, improving clinical results with savings in time and associated costs. This study focuses on studying the ability of heart failure patients with reduced ejection fraction (EF≤40%) to use a digital platform through an application installed on the patient's smartphone.

Status (registry)
Completed
Study type
Observational
Enrollment
6 (actual)
First submitted
24 Feb 2025
Start date
24 Feb 2025
Primary completion date
25 Jun 2025
Lead sponsor
Persei Vivarium
NCT number
NCT06869408

What you commit to

  • Study type: Observational
  • Participants enrolled: 6
  • From 24 Feb 2025 to the primary completion date, 25 Jun 2025
  • 1 site 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.

Other

  • Patients who will not be able to commit to carrying out the follow-ups or do not have adequate technological skills.
  • Patients with inability to give adequately the informed consent.

Who the study is looking for

  • Patients aged 18 years or older
  • Informed Consent is obtained from the patient
  • Patients diagnosed with heart failure with reduced ejection fraction (EF≤40%)
  • Patients who extensively use a smartphone.

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

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Hospital Universitario Son Llatzer
Coordinator of this site? Confirm its status
Palma de MallorcaSpainUnknown status

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