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. 2016 Apr 11;1(1):34–42. doi: 10.1016/j.ekir.2016.04.001

Figure 2.

Figure 2

iChoose Kidney Study schema shows the study process and points of data collection for both control and intervention patients, and clinical providers (i.e., nephrologists or surgeons). All patients will receive informed consent and a baseline survey before being evaluated by a transplant provider. Patients will complete a postconsultation survey after the provider consultation. Providers will receive a baseline survey prior to patient recruitment. After consulting with each patient, providers will take a postconsultation survey. At study completion, providers will complete a poststudy survey.