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Clinical Trial Summary

This prospective study will include both an intervention and control arm. The control arm will receive face-to-face pharmacy clinic visits per standard of care. The intervention arm will receive pharmacy clinic visits plus additional telephone follow-up. Patients with a hemoglobin A1c in the last 3 months greater than 9% will be eligible. Eligible patients must have a primary care physician at Johns Hopkins Outpatient Center (JHOC) or East Baltimore Medical Center (EBMC).

Purpose: To compare the change in hemoglobin A1c over the 3 month study period in the intervention group in which patients participate in telemedicine, to a control group in which they do not


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02344082
Study type Interventional
Source Johns Hopkins University
Contact
Status Completed
Phase N/A
Start date January 2015
Completion date June 2015

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