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NCT05529030 Clinical Trial

COVID-19 Booster Readiness Survey

Vaccination Refusal Clinical Trial

Official title:
COVID-19 Booster Readiness Survey

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05529030
Other study ID # 2022-0726
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2022
Est. completion date September 15, 2022

Study information
Verified date September 2022
Source Geisinger Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 12036
Est. completion date September 15, 2022
Est. primary completion date September 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Employee at the health system

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Salience of Omicron variant
The message mentions the Omicron variant, which can be a fear appeal or make salient the reason for the new booster
• Self-protection message
The message makes a reference to protecting one's self
• Other-protection message
The message makes a reference to protecting others (patients)

Locations
Country Name City State
United States Geisinger Clinic Danville Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
Geisinger Clinic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Count of employees who indicate interest in the booster Number of employees who indicate that they plan to get the booster when it is available 14 days
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