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临床试验/NCT01667354
NCT01667354已完成不适用

Vaccine Hesitancy Intervention--Provider (VHIP)

Kaiser Permanente2 个研究点 分布在 1 个国家目标入组 491 人开始时间: 2012年2月最近更新:
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
491
试验地点
2
主要终点
Parental Vaccine Hesitancy Measure

研究概览

简要总结

The primary aim of this trial is to test the effectiveness of an intervention to train primary care physicians to determine if it leads to decreased parental vaccine hesitancy.

详细描述

The primary aim of this trial is to test the effectiveness of an intervention to train primary care physicians to determine if it leads to decreased parental vaccine hesitancy. The investigators will train primary care teams with an initial training followed by telephone coaching and follow-up visits, and assess the outcomes of parental vaccine hesitancy (primary) and physician self-efficacy (secondary) at baseline and 6 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Intervention Clinics

Experimental

Providers in intervention clinics will receive a training followed by telephone coaching and follow-up visits for six months.

干预措施: Academic Detailing (Behavioral)

Control Clinics

No Intervention

Control clinics will receive all intervention materials at the completion of the study.

结局指标

主要结局

Parental Vaccine Hesitancy Measure

时间窗: Change from Baseline in Parental Hesitancy at 6 months

The investigators will contact mothers of newborns in study practices and conduct a telephone survey at two time points: baseline and 6 months. Surveys will assess parental hesitancy, parental trust in provider, and other covariates such as perceived social norms, other sources of information about vaccines, and demographic information.

次要结局

  • Physician Self Efficacy Measure(Change from Baseline in Physician Attitudes at 6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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