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临床试验/NCT04568590
NCT04568590已完成不适用

Cohort Study to Determine the Effect of an Educational Intervention Focusing on Herd Immunity to Enhance Vaccination Uptake Rates

Wake Forest University Health Sciences1 个研究点 分布在 1 个国家目标入组 510 人开始时间: 2020年10月19日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
510
试验地点
1
主要终点
Change in Vaccine Hesitancy Scores Pre- and Post-Intervention.

研究概览

简要总结

Subjects enrolled in this study are eligible for the seasonal influenza vaccine. The purpose of this research study is to figure out if increasing individuals' awareness of the benefits of herd immunity, specifically to the local pediatric oncology community, can improve vaccination uptake rates.

详细描述

The purpose of this study is to identify associations with influenza vaccine hesitancy, including parental demographics and altruism score, in families with healthy children attending two pediatric practices.

Also, in the cohort of families with baseline vaccine hesitancy, to assess the effectiveness of a pilot educational intervention focusing on the development of herd immunity for pediatric oncology patients by measuring:

  1. The change in vaccine hesitancy scores pre- and post-intervention.
  2. The rate of influenza vaccine uptake compared to historic controls from previous influenza seasons.

Another aim is to explore the relationship between baseline influenza vaccine hesitancy rates and baseline altruism scores. Effectiveness of this intervention is dependent on parental altruism levels; therefore, the study team also seeks to determine if there is an association between parental altruism and vaccine hesitancy for their children.

This is a single-arm prospective cohort study. The study will enroll legal guardians of children who are influenza vaccine-eligible to measure their vaccine hesitancy scores, altruism scores, and the impact of an educational intervention focused on herd immunity on the guardians' vaccine hesitancy score.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

性别
All
接受健康志愿者
是

入选标准

  • •All legal guardians of children aged 6 months and up who are influenza vaccine-eligible and present to the pediatric clinic.

排除标准

  • •Legal guardians of children who are not influenza vaccine-eligible including children less than 6 months of age, children on immunosuppressive medications, and children with underlying medical conditions resulting in an immunocompromised state.

研究组 & 干预措施

Vaccine Hesitant

Experimental

Subjects who consent to this study and deemed vaccine hesitant, they will receive an educational intervention.

干预措施: educational intervention (Behavioral)

结局指标

主要结局

Change in Vaccine Hesitancy Scores Pre- and Post-Intervention.

时间窗: Baseline (Pre-intervention) and Post-Intervention, up to 4 hours

8-item Vaccine Hesitancy Scale. Subjects identified as vaccine-hesitant based on a Vaccine Hesitancy Score \>/= 3. Score range is 1-5 and \> or = 3 is considered vaccine hesitant.

Pre-Intervention Vaccine Hesitancy Score

时间窗: baseline

8-item Vaccine Hesitancy Scale. Subjects identified as vaccine-hesitant based on a Vaccine Hesitancy Score \>/= 3. Score range is 1-5 and \> or = 3 is considered vaccine hesitant.

Post-Intervention Vaccine Hesitancy Score

时间窗: Post-Intervention up to 4 Hours

8-item Vaccine Hesitancy Scale. Subjects identified as vaccine-hesitant based on a Vaccine Hesitancy Score \>/= 3. Score range is 1-5 and \> or = 3 is considered vaccine hesitant.

次要结局

  • Pre-Intervention Altruism Scale(baseline)
  • Rate of Influenza Vaccine Uptake(baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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