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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01519570
Other study ID # 2010H0290
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 2011
Est. completion date December 2011

Study information

Verified date August 2018
Source Ohio State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Despite the significant benefits of herpes zoster vaccine (HZV), vaccination rates remain low. Electronic medical records (EMR) can serve as a practical strategy to better facilitate the application of preventative health care, such as increasing immunization rates. A new care model that can increase the herpes zoster vaccination rate, as well as other preventative health services, is warranted. The objective of this study is to investigate if the functions of an EMR, in combination with a pharmacist as part of the care team, can improve the herpes zoster vaccination rate.


Recruitment information / eligibility

Status Completed
Enrollment 2589
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria:

- Greater than 60 years of age

Exclusion Criteria:

- Documented herpes zoster vaccine in the EMR

Study Design


Related Conditions & MeSH terms


Intervention

Other:
An informational packet regarding shingles and the HZV was sent to patients identified by the EMR
The EMR generated a list of patients aged 60 or older without HZV documentation. Patients were categorized into two subgroups based on activated electronic patient portal (EPP) status. Randomized patients from each subgroup received an informational packet regarding shingles and the HZV by either the EMR or USPS mail, depending on EPP status. A pharmacist reviewed the medical chart of interested patients to assess if the HZV was clinically indicated; eligible patients were mailed a HZV prescription.

Locations

Country Name City State
United States The Ohio State University Martha Morehouse General Internal Medicine Clinic Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Ohio State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants Who Received the Herpes Zoster Vaccine Six months after the intervention, a second EMR report was generated to determine the change in vaccination rate of both the intervention and control groups. 6 months
Secondary Difference in Vaccination Rates Between Patients Who Recieved a Mailed Letter Versus a Secure Email Difference in vaccination rates between patients sent communications via US postal service (USPS) and those sent communications via electronic patient portal (EPP) 6 months
Secondary Amount of Time Required by a Clinical Pharmacist to Manage This Workflow 6 months