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

This study has been completed.
Sponsor:
Collaborators:
Merck
American Pharmacists Association
Information provided by:
University of Tennessee
ClinicalTrials.gov Identifier:
NCT00689013
First received: May 21, 2008
Last updated: April 22, 2009
Last verified: April 2009

May 21, 2008
April 22, 2009
February 2008
March 2008   (final data collection date for primary outcome measure)
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 ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00689013 on ClinicalTrials.gov Archive Site
  • To evaluate the relative efficacy of specific interventions on the rate of herpes zoster vaccinations [ Time Frame: 2 months ] [ Designated as safety issue: No ]
  • To evaluate the perception of patients receiving the herpes zoster vaccination as to the role of pharmacists as immunizers [ Time Frame: 2 months ] [ Designated as safety issue: No ]
Same as current
 
 
 
The Effect of Pharmacist Intervention on the Use of Zostavax in a Community Pharmacy Setting
The Effect of Pharmacist Intervention on the Use of Zostavax in a Community Pharmacy Setting

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.

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.

Interventional
 
Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Factorial Assignment
Masking: Open Label
Primary Purpose: Prevention
Herpes Zoster
  • Other: Personalized letter
    On Day 1 of the 2nd month, a personalized letter (addressing specific patient) was mailed to current pharmacy patients with indications for the Zostavax vaccine. Current patients were defined as those receiving at least one prescription medication from the pharmacy within 6 months. The personalized letter provided detailed information about herpes zoster infection, the vaccine for herpes zoster prevention, indications for vaccine receipt and contraindications for vaccine receipt.
    Other Name: Letter
  • Other: Flyer advertisement
    Beginning on Day 1 of the 2nd month, flyer advertisements were distributed with all pharmacy sales. Flyer advertisements provided detailed information about herpes zoster infection, the vaccine for herpes zoster prevention, indications for vaccine receipt and contraindications for vaccine receipt.
    Other Name: Flyer
  • Other: Newspaper press release
    During the first week of the 2nd month, local newspapers published press releases. The press release provided detailed information about herpes zoster infection, the vaccine for herpes zoster prevention, indications for vaccine receipt and contraindications for vaccine receipt.
    Other Name: Newspaper Ad
  • No Intervention: 1
    Patients voluntarily presenting to community pharmacies who request receipt of the herpes zoster vaccine during the first month of observation. These patients have not been exposed to pharmacist-driven interventions utilized in this study. This group serves as the control group.
  • Experimental: 2
    Patients voluntarily presenting to community pharmacies who request receipt of the herpes zoster vaccine during the second month of observation. These patients may or may not have been exposed to pharmacist-driven interventions utilized in this study. This group serves as the study/intervention group.
    Interventions:
    • Other: Personalized letter
    • Other: Flyer advertisement
    • Other: Newspaper press release
 

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
205
March 2008
March 2008   (final data collection date for primary outcome measure)

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
Both
60 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00689013
8750
No
Lindsay J. Ford, Pharm.D./Community Pharmacy Resident, University of Tennessee Community Pharmacy Residency Program
University of Tennessee
  • Merck
  • American Pharmacists Association
Principal Investigator: Lindsay J Ford, Pharm.D. University of Tennessee Community Pharmacy Residency Program
Study Chair: Sarah K Frank, Pharm.D. University of Tennessee Community Pharmacy Residency Program
Study Chair: Nina H Jaber, Pharm.D. University of Tennessee Community Pharmacy Residency Program
Study Director: Stephan L Foster, Pharm.D. University of Tennessee Community Pharmacy Residency Program
Study Chair: Richard Randolph, Pharm.D. University of Tennessee Community Pharmacy Residency Program
Study Chair: Steve Lane, Pharm.D. University of Tennessee Community Pharmacy Residency Program
Study Chair: Cindy T Smith, Pharm.D. University of Tennessee Community Pharmacy Residency Program
University of Tennessee
April 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP