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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02344082
Other study ID # IRB00051947
Secondary ID 1819
Status Completed
Phase N/A
First received
Last updated
Start date January 2015
Est. completion date June 2015

Study information

Verified date December 2018
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

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


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients with a primary care provider at JHOC or EMBC

- Patients have seen primary care provider within last 6 months

- Patients with hemoglobin A1c greater than 9%

Exclusion Criteria:

- Patients <18 years of age

- Patients with previously established care with JHH ambulatory care pharmacist

- Patients with communication barriers who do not have a caregiver

- Patients with new diagnosis of diabetes

- Patients who are pregnant or planning to become pregnant during the time of the study

- Patients followed by Endocrinology or Diabetes Center

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Telemedicine
The intervention arm will receive pharmacy clinic visits plus additional telephone follow-up.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Johns Hopkins University

Outcome

Type Measure Description Time frame Safety issue
Primary Change in hemoglobin A1c A1c at 3 months - A1c at Baseline 3 months
Secondary Patient adherence to office visits (# visits attended/# of visits scheduled) # visits attended/# of visits scheduled 3 months
Secondary Pharmacist interventions (Number of pharmacist interventions (lifestyle or medication changes) made) Number of pharmacist interventions (lifestyle or medication changes) made 3 months
Secondary Patient satisfaction (Based on survey results) Based on survey results at final pharmacy clinic visit 3 months
Secondary Telemedicine in Usual Care (Percent of patients who receive telephone call under usual care) Percent of patients who receive telephone call under usual care 3 months
Secondary Telemedicine Adherence (Percent of telephone encounters completed in intervention arm) Percent of telephone encounters completed in intervention arm 3 months
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