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The Do CHANGE 2 program implemented in this trial was similar to that described by Broers et al for Do CHANGE 1 [20]. Patients randomized to the intervention group received devices for measuring key clinical parameters needed for monitoring their CVD, such as a BP monitor, weight scale (in HF patients only), and the Careportal, which allowed monitoring of daily symptoms and an electrocardiogram. The patient’s location was monitored by the Moves app.
J Med Internet Res 2020;22(7):e17351
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