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Clinical Trials/NCT00689013
NCT00689013
Completed
N/A

The Effect of Pharmacist Intervention on the Use of Zostavax in a Community Pharmacy Setting

University of Tennessee3 sites in 1 country205 target enrollmentFebruary 2008
ConditionsHerpes Zoster

Overview

Phase
N/A
Intervention
Not specified
Conditions
Herpes Zoster
Sponsor
University of Tennessee
Enrollment
205
Locations
3
Primary Endpoint
To assess the effect of a pharmacist-driven immunization campaign on the rate of Zostavax immunizations in three separate community pharmacy settings
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The purpose of this study is to determine whether pharmacist-driven patient interventions can have an effect on the number of herpes zoster (Zostavax) vaccinations given in a community pharmacy setting.

Detailed Description

Several studies exist documenting the perception and satisfaction of patients receiving immunizations from pharmacists, as well as the effects of pharmacist involvement in advocating and administering vaccinations. The most well documented studies have been conducted in hospital settings. Undoubtedly, there is enormous opportunity for the community pharmacist to identify potential vaccine recipients, advocate immunization and administer said immunizations to their established patient populations. However, there is a lack of concentrated study in the implementation of immunization services in the community setting and their effects. The investigators intend to evaluate the intervention of pharmacists in an immunization program and the resulting changes in immunization rates.

Registry
clinicaltrials.gov
Start Date
February 2008
End Date
March 2008
Last Updated
17 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • men and women aged 60 or older without contraindications for the herpes zoster vaccination
  • patients who have already experienced one or more episodes of herpes zoster infection were considered for vaccine receipt and study inclusion secondary to CDC ACIP recommendations

Exclusion Criteria

  • Patients aged \< 60 years
  • Anyone who has previously received the herpes zoster vaccine
  • Anyone with an allergy to neomycin, gelatin or any other component of the vaccine
  • Anyone receiving a live vaccine within 4 weeks
  • Anyone with a compromised or weakened immune systems such as those receiving radiation, corticosteroids, or those with HIV/AIDS, cancer in the lymph, bone or blood systems
  • Pregnant women or those in close contact with a pregnant woman

Outcomes

Primary Outcomes

To assess the effect of a pharmacist-driven immunization campaign on the rate of Zostavax immunizations in three separate community pharmacy settings

Time Frame: 2 months

Secondary Outcomes

  • To evaluate the relative efficacy of specific interventions on the rate of herpes zoster vaccinations(2 months)
  • To evaluate the perception of patients receiving the herpes zoster vaccination as to the role of pharmacists as immunizers(2 months)

Study Sites (3)

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