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Clinical Trials/NCT05508698
NCT05508698CompletedNot Applicable

Pre-visit Questionnaire to Increase Influenza Vaccinations

Geisinger Clinic1 site in 1 country230,962 target enrollmentStarted: August 18, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
230,962
Locations
1
Primary Endpoint
Count of patients with a flu vaccination

Study Overview

Brief Summary

The purpose of this study is to assess, prospectively, the effect on flu vaccination rates of a pre-visit questionnaire that asks patients to indicate their preferences for a flu shot. Responses to the questionnaire will also be shown to clinicians via additional text in an existing flu shot alert. The investigators hypothesize that the pre-visit questionnaire will lead to increased flu vaccination compared with standard practices.

Detailed Description

The CDC (Centers for Disease Control and Prevention) recommends a flu vaccination to everyone aged 6+ months, with rare exception; almost anyone can benefit from the vaccine, which can reduce illnesses, missed work, hospitalizations, and death. One barrier to vaccination is a lack of "cues to action," which could be overcome by asking patients for a pre-visit commitment to get a flu shot and additional reminders for the clinician to act on this commitment.

Eligible patients will be randomized to either receive or not receive a one-item, pre-visit questionnaire about the flu shot (that will show responses to clinicians in an existing flu shot alert).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Masking Description

Patient-participants will not be explicitly told about the different arms, although clinician-participants will see the different arms and may notice these differences.

Eligibility Criteria

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

Inclusion Criteria

  • •On a list of active Geisinger patients (all patients on this list attended at least one primary care appointment at Geisinger between 10/1/2008 and 4/13/2022, and either had a Geisinger primary care provider assigned as of April 2022, or were in the Electronic Health Record [EHR] since at least September 2021 and had at least one encounter in 2020-2022)
  • •Has an upcoming flu shot-eligible outpatient visit with a provider
  • •Has activated Geisinger's patient portal
  • •Has not yet received a flu vaccine at the time the questionnaire became available, according to the EHR
  • •Clinician Inclusion Criteria
  • •Any Geisinger clinician who sees patient-participants in our study for a flu shot-eligible outpatient visit

Exclusion Criteria

  • Not provided

Arms & Interventions

Passive Control

No Intervention

No change to the standard of care for flu vaccines

Pre-visit Questionnaire

Experimental

One-item questionnaire in online patient portal and additional information in the flu shot alert

Intervention: Precommitment Nudge (Behavioral)

Pre-visit Questionnaire

Experimental

One-item questionnaire in online patient portal and additional information in the flu shot alert

Intervention: Salience (Behavioral)

Outcomes

Primary Outcomes

Count of patients with a flu vaccination

Time Frame: Up to 21 days

Patient received a flu vaccine (yes/no) between the day questionnaires became available for the patient's first scheduled flu-shot-eligible appointment and 7 days following the appointment. Questionnaires were available 14 days prior to the appointment date for appointments scheduled at least 14 days in advance. Questionnaires were available on the day the appointment was scheduled for appointments scheduled less than 14 days in advance. Note that control patients did not receive a flu shot questionnaire, but they may have received other questionnaires from the health system 14 days before their appointment. We will conduct subgroup analyses for people who had responded to MyGeisinger pre-visit messages in the previous year and those who did not.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Christopher F Chabris, PhD

Professor

Geisinger Clinic

Study Sites (1)

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