Heart Failure Clinical Trial

e-Diary in Heart Failure

Summary

The purpose of this study is to determine the efficacy and feasibility of using a smartphone application to monitor symptoms and weight in patients with advanced heart failure.

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Full Description

Attention to symptoms of heart failure and weight gain are central tenets in heart failure patient education and self-care. A key self-care skill for heart failure patients is the early detection of subtle changes in symptoms. Daily diary use can be one method for patients to acknowledge and attend to their symptoms. This study is examining if the use of a diary in the form of an app on a mobile phone will improve patient outcomes. Participants will be randomized to one of two groups-- usual care or the Movn mobile application. Participants randomized to the mobile app will be asked to record their weight and any symptoms every day over the course of two months.

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Eligibility Criteria

Inclusion Criteria:

At least 18 years old
History of symptomatic heart failure (Class III or IV)
Owns a smartphone or tablet compatible with the Movn mobile application

Exclusion Criteria:

Cognitive impairment
Lack of English proficiency/literacy
Clinically unstable (decompensated heart failure NYHA class 3-4; unstable arrhythmias, aortic stenosis, thrombophlebitis, dissecting aneurysm, or symptomatic anemia; active infection; uncontrolled blood pressure: resting diastolic higher than 100 mmHg, systolic greater than 180 mmHg; unstable angina, 2nd or 3rd degree heart block; or uncontrolled high grade exercise-induced ventricular ectopy or hemodynamically unstable)

Study is for people with:

Heart Failure

Study ID:

NCT03452683

Recruitment Status:

Withdrawn

Sponsor:

University of California, San Francisco

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There is 1 Location for this study

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John Muir Medical Center
Concord California, 94520, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Study ID:

NCT03452683

Recruitment Status:

Withdrawn

Sponsor:


University of California, San Francisco

How clear is this clinincal trial information?

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