Telemedicine
OtherThe intervention arm will receive pharmacy clinic visits plus additional telephone follow-up.
NCT Number: NCT02344082
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
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The intervention arm will receive pharmacy clinic visits plus additional telephone follow-up.
Time frame: 3 months
A1c at 3 months - A1c at Baseline
Time frame: 3 months
# visits attended/# of visits scheduled
Time frame: 3 months
Number of pharmacist interventions (lifestyle or medication changes) made
Time frame: 3 months
Based on survey results at final pharmacy clinic visit
Time frame: 3 months
Percent of patients who receive telephone call under usual care
Time frame: 3 months
Percent of telephone encounters completed in intervention arm
Johns Hopkins University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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