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Use of an Electronic Medical Record in the Primary Care Setting to Improve Herpes Zoster Vaccination Rates

Use of an Electronic Medical Record to Improve Standard Practice in the Primary Care Setting: A Randomized-Controlled Study of Herpes Zoster Vaccination Rates

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01519570
Enrollment
2589
Registered
2012-01-27
Start date
2011-03-31
Completion date
2011-12-31
Last updated
2019-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Herpes Zoster Disease

Keywords

Herpes Zoster vaccine, Electronic patient portal, Electronic medical record, Primary care, Immunizations

Brief 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.

Interventions

OTHERAn 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.

Sponsors

Ohio State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Greater than 60 years of age

Exclusion criteria

* Documented herpes zoster vaccine in the EMR

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants Who Received the Herpes Zoster Vaccine6 monthsSix months after the intervention, a second EMR report was generated to determine the change in vaccination rate of both the intervention and control groups.

Secondary

MeasureTime frameDescription
Difference in Vaccination Rates Between Patients Who Recieved a Mailed Letter Versus a Secure Email6 monthsDifference in vaccination rates between patients sent communications via US postal service (USPS) and those sent communications via electronic patient portal (EPP)
Amount of Time Required by a Clinical Pharmacist to Manage This Workflow6 months

Countries

United States

Participant flow

Participants by arm

ArmCount
An Informational Packet Regarding Shingles and the HZV
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.
500
Standard Medical Care From Their Primary Care Physician2,089
Total2,589

Baseline characteristics

CharacteristicStandard Medical Care From Their Primary Care PhysicianAn Informational Packet Regarding Shingles and the HZVTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
2089 Participants500 Participants2589 Participants
Age, Categorical
Between 18 and 65 years
0 Participants0 Participants0 Participants
Age, Continuous73.1 years
STANDARD_DEVIATION 8.1
72.1 years
STANDARD_DEVIATION 9.4
72.8 years
STANDARD_DEVIATION 8.7
Region of Enrollment
United States
2089 participants500 participants2589 participants
Sex: Female, Male
Female
1174 Participants265 Participants1439 Participants
Sex: Female, Male
Male
915 Participants235 Participants1150 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 5000 / 2,089
serious
Total, serious adverse events
0 / 5000 / 2,089

Outcome results

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.

Time frame: 6 months

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
An Informational Packet Regarding Shingles and the HZVNumber of Participants Who Received the Herpes Zoster Vaccine500 Participants
Standard Medical Care From Their Primary Care PhysicianNumber of Participants Who Received the Herpes Zoster Vaccine2089 Participants
Secondary

Amount of Time Required by a Clinical Pharmacist to Manage This Workflow

Time frame: 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)

Time frame: 6 months

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026