To understand the feasibility of characterizing walking patterns in heart failure subjects and subjects at risk for arrhythmias using an investigational wearable monitor called the SWAN study system.
This is a non-randomized, feasibility study that will enroll up to 60 participants diagnosed with Class II (30-35%) or III (30-35%) heart failure or are indicated for an insertable cardiac monitor with no history of heart failure (30-35%). There will be one study visit per participant and a follow up phone call. The study visit includes device placement and data collection during rest and during a 6 minute hall walk. The device will then be removed.
Study Type
OBSERVATIONAL
Enrollment
40
Participants will be fitted with a wearable cardiac monitor placed on their skin that measures physiological signals.
CentraCare Heart and Vascular Clinic
Saint Cloud, Minnesota, United States
Step Detection
Characterize step count in class II and III heart failure and in ICM indicated patients with no history of heart failure.
Time frame: 12 months
Walking Patterns
Characterize walking patterns in class II and III heart failure and in ICM indicated patients with no history of heart failure.
Time frame: 12 months
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