Using a monitoring system to improve care for patients with chronic heart failure
Feasibility and Efficacy Study of the CardioPulmonary Monitoring (CPM) System in Patients With Chronic Heart Failure
This study is testing if a new monitoring system can help people with chronic heart failure feel better and reduce hospital visits while also making their care more satisfying.
Quick facts
| Phase | Phase2; Phase3 |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Analog Device, Inc. Academic / other |
| Locations | 1 site (Greenville, South Carolina) |
| Trial ID | NCT05978518 on ClinicalTrials.gov |
What this trial studies
This study evaluates the feasibility and efficacy of the CardioPulmonary Monitoring (CPM) system in patients with chronic heart failure. It aims to determine whether the CPM system can reduce heart failure-related events and healthcare costs while improving quality of care and patient satisfaction. Participants will be randomized into two groups: one receiving the CPM system with physician data review and the other using the system without data review. The study will monitor patient outcomes over a six-month period, assessing the impact of the CPM system on their health and healthcare utilization.
Who should consider this trial
Good fit: Ideal candidates include heart failure patients of any ejection fraction with NYHA Class II-IV symptoms and specific comorbidities.
Not a fit: Patients under 18, those with severe COPD, or cognitive impairments that hinder device use may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management of chronic heart failure, reducing hospitalizations and healthcare costs for patients.
How similar studies have performed: Other studies have shown promise in using monitoring systems for chronic conditions, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Heart failure patients regardless of ejection fraction (HFpEF or HFrEF) with one or more of the following: * NYHA Class III-IV * NYHA Class II HF with one or more of the following: * Chronic Kidney Disease (eGFR\<60 within the past 6 months) * HF hospitalization (defined as HF listed as the major reason for hospitalization) within 9 months prior to screening visit and NT-proBNP \> 200 pg/ml for patients not in AF or \> 600 pg/m for patients in AF on screening ECG * NT-proBNP \> 300 pg/ml for patients not in AF or \> 900 pg/ml for patients in AF on the screening visit ECG. * Chronic obstructive pulmonary disease (COPD) Exclusion Criteria: * Under 18 years of age * Patients with severe COPD (GOLD stage III or IV) * Limited mobility preventing application of device * Cognitive impairments that would limit the application and proper use of the device * Skin allergies or skin sensitivities to silicone-based adhesives * Pregnancy * Skin breakdown on the left chest or breast area * Not willing to shave chest hair if needed to apply device * Patients on chronic ionotropic therapy * Patients with any condition that might limit the survival to less than 1 year as assessed by the investigator * No cellular coverage (Patient's Home)
Where this trial is running
Greenville, South Carolina
- Prisma Health — Greenville, South Carolina, United States (Recruiting)
Study contacts
- Study coordinator: Emily Wycallis
- Email: emily.wycallis@analog.com
- Phone: 9784351644
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.