HF-TRACK: A UK RCT of an Passive Heart Failure Monitoring and Tracking Device

Inclusion Criteria

• •In order to be eligible to participate in this trial, an individual must meet all of the following criteria:
• •Provision of signed and dated informed consent form (e-consent via website or app is acceptable).
• •Women or men, aged 18 years or older \[No maximum age\].
• •Diagnosis of heart failure at least 3 months previously
• •Receiving diuretics on a daily basis
• •Peripheral oedema reported on at least one HF-related hospitalisation in the last 4 years (as documented in EPR).
• •Hospitalised for HF OR on a Virtual Ward for HF OR has received IV diuretic treatment in the last 12 months, or treated with at least 80 mg furosemide (or equivalent) orally per day.
• •For women of reproductive potential: use of highly effective contraception for at least 1 month prior to screening and agreement to use such a method during study participation and for an additional 6 weeks after the end of the study.
• •Is considered by the investigator to be non-adherent OR at high risk of HF hospital readmissions.