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Improving Shingrix Vaccination Among US Veterans Receiving Immunosuppression

VA Quality Improvement Research and Training Initiative

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06596148
Enrollment
130
Registered
2024-09-19
Start date
2024-09-16
Completion date
2026-06-30
Last updated
2025-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Immunosuppresion

Keywords

Wait-list control randomized trial

Brief summary

The goal of this wait-list control trial is to learn if having access to a new dashboard displaying information about immunosuppressed Veterans missing vaccinations for Shingrix can improve Shingrix vaccination rates at VA facilities. The main question\[s\] it aims to answer is: Will vaccination rates improve more rapidly for facilities with access to the dashboard compare to facilities without access? VA facility personnel will be granted access to the dashboard and outcomes (vaccination rates) will be measured using electronic health record data.

Detailed description

Assignment of the intervention will occur at the facility level. Outcomes (vaccination) will be assessed for patients cared for at each facility.

Interventions

OTHERAccess to Shingrix dashboard

The investigators will build and grant access to a clinical dashboard that exists behind the VA firewall. The dashboard will identify Veterans from each VA facility who are receiving immunosuppressants (prescribed via the VA). The dashboard will also provide information about the number of Shingrix vaccines each patient has received (which have been documented within the VA electronic health record). VA clinicians will have access to view information about patients based on their VA electronic health record permissions.

Sponsors

San Francisco Veterans Affairs Medical Center
CollaboratorFED
University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

The investigators will use a wait-list control design; clinicians from VA facilities will be randomized to receive access to the dashboard early vs. after a 6-9 month delay. The investigators will compare Shingrix vaccination rates in the two groups of facilities.

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* In order to be included in the study, clinicians need to work at a VHA facility and have access to the electronic health record.

Exclusion criteria

* None.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of patients with at least 1 Shingrix vaccine documented, by facilityFrom enrollment until end of follow up at 18 months.Percentage of patients with at least 1 Shingrix vaccinations documented, by facility

Secondary

MeasureTime frameDescription
Percentage of patients with at least 2 Shingrix vaccinations documented, by facilityFrom enrollment until end of follow up at 18 months.Percentage of patients with at least 2 Shingrix vaccinations documented, by facility

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026