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As this was a pilot study, a convenience sample was used, consisting of patients who had scheduled outpatient visits over the course of a 4-month period between February and May 2013.
Patients were deemed eligible if they were ambulatory, English-speaking adults ≥18 years of age with a current diagnosis of heart failure. Patients were required to have regular access to a telephone and be able to navigate a simple website, understand the scope of the study, and provide written informed consent.
JMIR Mhealth Uhealth 2015;3(2):e33
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