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

NCT00689013 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 205

Last updated 2009-04-23

No results posted yet for this study

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.

Conditions

  • Herpes Zoster

Interventions

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

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

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.

Sponsors & Collaborators

  • Merck Sharp & Dohme LLC

    collaborator INDUSTRY
  • American Pharmacists Association

    collaborator OTHER
  • University of Tennessee

    lead OTHER

Principal Investigators

  • Lindsay J Ford, Pharm.D. · University of Tennessee Community Pharmacy Residency Program

  • Sarah K Frank, Pharm.D. · University of Tennessee Community Pharmacy Residency Program

  • Nina H Jaber, Pharm.D. · University of Tennessee Community Pharmacy Residency Program

  • Stephan L Foster, Pharm.D. · University of Tennessee Community Pharmacy Residency Program

  • Richard Randolph, Pharm.D. · University of Tennessee Community Pharmacy Residency Program

  • Steve Lane, Pharm.D. · University of Tennessee Community Pharmacy Residency Program

  • Cindy T Smith, Pharm.D. · University of Tennessee Community Pharmacy Residency Program

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-02-29
Primary Completion
2008-03-31
Completion
2008-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00689013 on ClinicalTrials.gov