Comparison of Two Pharmacist-led Population Management Approaches to Increase Monitoring of Vitamin B12 and Serum Creatinine Levels for Patients on Metformin
- Conditions
- Vitamin B12 DeficiencyNeuropathyType 2 DiabetesAnemia
- Interventions
- Behavioral: Office visit interventionBehavioral: Electronic Message Intervention
- Registration Number
- NCT02076347
- Lead Sponsor
- Ohio State University
- Brief Summary
The purpose of this project is to compare two pharmacist-led population management strategies designed to increase the rate of appropriate monitoring of vitamin B12 and serum creatinine for patients taking metformin.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 489
- On Metformin for at least one year
- Activated patient portal for electronic messaging
- Patient of an attending physician at Ohio State General Internal Medicine
- No serum vitamin B12 and/or no serum creatinine measurement in the past year
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Office visit-based intervention Office visit intervention - Electronic message-based intervention Electronic Message Intervention -
- Primary Outcome Measures
Name Time Method Percentage of patients in each arm who obtain monitoring of vitamin B12 as recommended 6 months
- Secondary Outcome Measures
Name Time Method Number of patients with newly identified vitamin B12 deficiency 6 months Percentage of patients with newly identified vitamin B12 deficiency who have prior evidence of anemia upon chart review within 6 months When a patient's serum vitamin B12 level comes back and is low the chart will be reviewed immediately to determine this. This could happen anytime during the 6 month study period.
Percentage of patients with newly identified vitamin B12 deficiency who have prior evidence of neuropathy upon chart review within 6 months When a patient's serum vitamin B12 level comes back and is low the chart will be reviewed immediately to determine if neuropathy is also listed as a medical problem. This could happen anytime during the 6 month study period.
Trial Locations
- Locations (1)
The Ohio State University General Internal Medicine
🇺🇸Columbus, Ohio, United States