Heart Failure Clinical Trial

Integrated Tele-monitoring and Patient-centric Health Coaching Strategy in Patients Hospitalized With Heart Failure

Summary

This study evaluates the effectiveness of remote tele-monitoring and health coaching in helping to reduce hospitalizations in heart failure patients. Half of participants will receive tele-monitoring and health coaching, while the other half will receive standard health care provided by their chosen provider.

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Full Description

Tele-monitoring involves a personal monitoring system used to analyze data to provide relevant health information back to the treating clinician and the user. The monitoring system remotely monitors electrocardiographic (ECG) signals, heart rate, breathing rate, and activity levels. Additional devices will be integrated with the monitoring device to assess blood pressure and weight.

Health Coaching involves a team of health care professionals including a registered nurse (RN). The health care team creates a plan specific to the patient and provides guidance on nutrition' medications, and exercise. The data collected by the remote monitoring device will assist the care team in patient management.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Hospitalized with primary or secondary diagnosis of Acute Decompensated Heart Failure (one or more of these symptoms: shortness of breath, orthopnea or edema AND one or more of these signs: rales, peripheral edema, ascites, or pulmonary vascular congestion on chest radiography)
Adult patients >18 years old

Exclusion Criteria:

Overall life expectancy < 1 year
Known skin allergy to adhesives (hydrocolloid, silicone, acrylic)
Active systemic infection
Pregnant or lactating
End stage renal disease on dialysis
Subject or caregiver is not visually and tactile capable of smartphone and home device usage
Inadequate cell phone coverage (including international patients or international travel during study period)
Subject or legal guardian is not willing and able to provide appropriate informed consent

Study is for people with:

Heart Failure

Estimated Enrollment:

112

Study ID:

NCT02391987

Recruitment Status:

Completed

Sponsor:

Mayo Clinic

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There are 5 Locations for this study

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Mayo Clinic
Jacksonville Florida, 32224, United States
Memorial Regional Medical Center
Mechanicsville Virginia, 23116, United States
St. Francis Medical Center
Midlothian Virginia, 23114, United States
St. Mary's Hospital
Richmond Virginia, 23226, United States
Mayo Clinic Health Systems
La Crosse Wisconsin, 54601, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

112

Study ID:

NCT02391987

Recruitment Status:

Completed

Sponsor:


Mayo Clinic

How clear is this clinincal trial information?

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