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This sheet stated, “By continuing, I agree to take part in this study,” with a waiver for signed consent. Study data were deidentified. Patients and caregivers received US $50 for participation in phase 1.
Patients who completed treatment of colorectal cancer and health care professionals involved with colorectal cancer care were targeted for this application development. The study workflow is shown in Figure 1.
JMIR Form Res 2023;7:e41354
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Patient 3 specifically responded that he or she would not want to wear a cell phone while running saying “I think it would be difficult, so no.” While not considered a particular theme, 1 patient also made comments relating to specific concerns about privacy, professional life, and intimacy. As part of wearability, patients also specifically noted the battery life of the wrist device. While Patient 1 was able to charge the device and i Phone nightly, Patients 2 and 3 had some trouble.
JMIR Med Inform 2018;6(4):e46
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