Impact and Cost of a Pharmacist Pneumococcal Vaccination Program With PNEUMOVAX® 23 at an Urban Senior Center (PPVP)

May 26, 2017 updated by: Thomas Jefferson University

Impact and Cost of a Pharmacist Pneumococcal Vaccination Program With PNEUMOVAX® 23 at an Urban Senior Center for Adults Aged 65 Years or Older or Those With Defined Risk Factors for Invasive Pneumococcal Disease

The overall goals of this program are to measure the impact of a pharmacist pneumococcal vaccine education program (PPVP) using a senior center model of care and provide the pneumococcal vaccine to eligible participants.

Hypotheses

  1. PPVP will result in improved knowledge and awareness in older minorities in the senior center setting (primary hypothesis);
  2. Participants who are vaccinated through the project will experienced increased trust in receiving vaccines from a pharmacist;
  3. Participants will be satisfied with and trust the PV information provided by pharmacists in the PPVP;
  4. PPVP is an efficient approach to educating patients in the senior center based on its costs;
  5. Participating pharmacists will be activated to implement PPVP learnings in their practice.

Study Overview

Study Type

Interventional

Enrollment (Actual)

203

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19144
        • Center in the Park

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

50 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

A. Inclusions for PPVP:

  1. Age ≥ 50 years old
  2. Can attend a 1.5-hour session at CIP
  3. Cognitively intact based on responses to an Abbreviated Mental Test Score (AMTS) of ≥7 (see Appendix for AMTS instrument)
  4. Can speak and read English at ≥4th grade level as evidenced by ability to read a brief passage
  5. Access to a telephone

B. Inclusions to receive the optional pneumococcal vaccination:

Patient meets ≥1 of the following criteria for receiving their first pneumococcal vaccination:

  1. All adults age 65 years and older who have not had the vaccine previously
  2. Age 50-64 years with any of the following conditions:

    1. Cigarette smokers age 19 years and older
    2. Chronic cardiovascular disease (e.g., congestive heart failure, cardiomyopathies; excluding hypertension)
    3. Chronic pulmonary disease (including COPD and emphysema, and for adults ages 19 years and older, asthma)
    4. Diabetes mellitus
    5. Alcoholism
    6. Chronic liver disease, cirrhosis
    7. Candidate for or recipient of cochlear implant
    8. Functional or anatomic asplenia (e.g., sickle cell disease, splenectomy)
    9. Immunocompromising conditions or on immunosuppressive therapy
    10. Chronic renal failure or nephrotic syndrome

OR

Patient meets ≥1 of the following criteria for receiving a booster dose of the pneumococcal vaccination:

  1. Adults age 65 years and older who received their first dose for any indication when they were younger than age 65 years.
  2. Adults age 50-64 who have not received the vaccine for ≥5 years and have one of the following conditions:

    1. Functional or anatomic asplenia (including persons with sickle cell disease or splenectomy patients);
    2. Chronic renal failure (including dialysis patients) or nephrotic syndrome;
    3. Immunocompromising conditions or on immunosuppressive therapy

Exclusion Criteria:

A. Exclusions to the PPVP program: none

B. Exclusions to receiving the optional pneumococcal vaccine:

  1. Participant has a history of allergic reaction to pneumococcal vaccine
  2. Participant has a history of allergic reaction to any component of any vaccine
  3. Participant with moderate or severe illness (these individuals will be advised to speak to their doctor regarding the vaccine)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Pharmacist Pneumococcal Vaccine Program (PPVP)
Individuals receiving the PPVP intervention which consists of the educational program delivered on site at the collaborating senior center.
1.5 hour educational intervention delivered onsite at collaborating senior center consisting of 3 components: presentation about pneumococcal disease and the vaccine given by a infectious disease-certified pharmacist; 2) skits given by volunteer actors at the senior center to illustrate real world scenarios related to pneumococcal disease and the vaccine; 3) action planning to consist of small group breakouts led by licensed pharmacists and 4) vaccination day which is an optional component following the education program, for participants eligible to receive the vaccine. Vaccination to be provided free of charge to eligible participants who opt to receive it.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knowledge and Awareness of Pneumococcal Disease
Time Frame: Baseline, post-test, 3 months
Change in knowledge and awareness of pneumococcal disease over time were assessed for the following domains: susceptibility to infection, symptoms of disease, severity of illness, and vaccination with an emphasis on vaccine efficacy, safety, and eligibility. Assessments at baseline, post-test (immediately following intervention), and 3 months using the Pneumonia Knowledge Questionnaire, an instrument developed by investigators to assess participants' knowledge and awareness in the domains of interest. Instrument consists of 5 "mark all that apply" items and one "mark the best response" item. Scores range from 0 (no correct responses) to 28 (all responses correct), with a higher score value corresponding to better knowledge and awareness.
Baseline, post-test, 3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Trust in Pharmacists as Vaccine Providers
Time Frame: Baseline, post-test (immediately following intervention), 3 months
Trust in pharmacists as vaccine providers were measured by comparing responses to the trust items in the baseline, post-test (immediately following intervention), and 3-month assessments. Trust items were coded on a 4-level Likert scale, with lower values corresponding to higher agreement with the trust statements (therefore a lower mean response indicates greater trust). Minimum possible score was 1 (indicating complete trust in pharmacists as vaccine providers) and maximum possible score was 4 (indicating complete lack of trust in pharmacists as vaccine providers).
Baseline, post-test (immediately following intervention), 3 months
Activation
Time Frame: 3 months
Activation was measured as number of participants having taken action at 3 months or planning action at baseline, post-test, and 3 months.
3 months
Satisfaction With PPPP
Time Frame: 3 months
Satisfaction with PPPP was measured as participants' overall satisfaction with the content of PPPP, extent to which the participant felt engaged, and belief that the program helped them learn about pneumonia and the vaccination.
3 months
Intervention Cost
Time Frame: 3 months
Measures PPPP intervention costs per participant. Consists of total program costs divided by number of participants. Value reported is the per-participant cost with measure type "number".
3 months
Pharmacist Satisfaction
Time Frame: 3 months
Pharmacists who participated in the intervention were surveyed to determine their satisfaction with the program, including: 1) satisfaction with live action skit, 2) belief that PPPP was successful in educating participants, 3) belief that PPPP was successful in building trust in pharmacists among participants, 4) belief that PPPP was successful in increasing acceptance of pharmacists as immunizers, and 5) belief that PPPP will decrease barriers to vaccination among participants.
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Laura Pizzi, PharmD, MPH, Thomas Jefferson University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2014

Primary Completion (Actual)

November 1, 2014

Study Completion (Actual)

November 1, 2014

Study Registration Dates

First Submitted

September 5, 2013

First Submitted That Met QC Criteria

September 16, 2013

First Posted (Estimate)

September 17, 2013

Study Record Updates

Last Update Posted (Actual)

January 3, 2018

Last Update Submitted That Met QC Criteria

May 26, 2017

Last Verified

May 1, 2017

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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