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COVID-19 Booster Readiness Survey

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Geisinger Health

Status

Completed

Conditions

Vaccination Refusal

Treatments

Behavioral: Salience of Omicron variant
Behavioral: Self-protection message
Behavioral: Other-protection message

Study type

Interventional

Funder types

Other

Identifiers

NCT05529030
2022-0726

Details and patient eligibility

About

The purpose of this administrative survey is to inform health system logistics by assessing the attitudes towards towards the bivalent COVID-19 boosters held by healthcare workers (HCWs) at a large, rural health system. It will also test, prospectively, the effect on interest in the bivalent COVID-19 booster of different framing approaches in a survey question sent to employees of a large, rural health system.

Full description

The Food and Drug Administration has authorized two bivalent COVID-19 boosters with the expectation that the Centers for Disease Control will soon recommend them. The researchers plan to survey the HCWs at a large, rural health system on their attitudes on the bivalent booster.

This survey will gather data on HCWs' interest in a bivalent booster, reasons for hesitancy, risk perception about COVID-19 infection and its complications, and prior COVID-19 infection and vaccination.

Respondents will also be randomly assigned to see different versions of the question asking if they are interested in a bivalent booster with different framing approaches, such as protection of the self or protection of patients (for patient-facing employees). Information on prior vaccination and perceptions of risk will also be gathered and used as covariates in the analysis.

Enrollment

12,036 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Employee at the health system

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

12,036 participants in 4 patient groups

Standard question
No Intervention group
Description:
Question with no additional text or framing
Question with salient Omicron message
Experimental group
Description:
Question indicates that the bivalent booster can protect the respondent from the Omicron variant
Treatment:
Behavioral: Self-protection message
Behavioral: Salience of Omicron variant
Question with patient protection message
Experimental group
Description:
Question indicates that the bivalent booster can protect patients (only presented to patient-facing employees)
Treatment:
Behavioral: Other-protection message
Question with salient Omicron and patient protection message
Experimental group
Description:
Question indicates that the bivalent booster can protect patients from the Omicron variant (only presented to patient-facing employees)
Treatment:
Behavioral: Salience of Omicron variant

Trial documents
1

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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