The primary purpose for this study is to support the hypothesis (pilot data) that the use of the Sensinel CPM system reduces the rate of HF-related events and the related healthcare cost. The study will also measure the impact on quality of care and patient satisfaction. In order to support the primary objective, the study will compare the outcomes and costs for patients using the Sensinel CPM system against those who are not. This can either be done using institutions' averages, if available, or through a control group.
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Admission Rate
Timeframe: 7 months
Readmission Rate
Timeframe: 7 months
Healthcare Utilization
Timeframe: 7 months
Patient satisfaction
Timeframe: 6 months
Cost of care
Timeframe: 7 months (during study) and 12 months prior to the study
Quality of care
Timeframe: 6 months