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Clinical Trials/NCT03372967
NCT03372967CompletedNot Applicable

Project IMPACT Immunizations (IMProving America's Communities Together) Scaled Demonstration

American Pharmacists Association Foundation12 sites in 1 country6,234 target enrollmentStarted: December 12, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
6,234
Locations
12
Primary Endpoint
Change in vaccination rates for routinely recommended adult vaccinations

Study Overview

Brief Summary

The primary objective of this study is to evaluate how implementing an innovative care model that provides the pharmacist access to a patient's vaccine history at the point-of-care impacts the pharmacist's ability to identify unmet vaccination needs and increase vaccination rates for routinely recommended adult vaccinations.

Detailed Description

This multi-site study will use a pre-post design with a population-based comparison group to investigate the impact of implementing an innovative care model on the pharmacist's ability to identify unmet vaccination needs and increase vaccination rates for routinely recommended adult vaccinations. The innovative care model enables the pharmacist to utilize a bi-directional IIS to assess patients' vaccination histories, identify unmet vaccination needs, and document the care provided. The project duration has been established to allow sufficient time for each pharmacy to implement the innovative care model and monitor each pharmacy for a 6-month study period. The American Pharmacists Association (APhA) Foundation has an a priori intent to publish the project results.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Individuals eligible to be enrolled in the study include any person at least 18 years of age who is eligible for a comprehensive vaccination history review as determined by the pharmacist.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in vaccination rates for routinely recommended adult vaccinations

Time Frame: 6 months

Change from baseline rates

Secondary Outcomes

  • Number of vaccines administered(6 months)
  • Types of vaccines administered(6 months)
  • Number of unmet vaccination needs that were identified and met(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (12)

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