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临床试验/NCT03111251
NCT03111251已完成不适用

Multi-component Interventions for Patients and Providers to Increase HPV Vaccination in a Network of Pediatric Clinics in Houston, TX

The University of Texas Health Science Center, Houston2 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2015年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,000
试验地点
2
主要终点
Change in percent of HPV vaccination initiation

研究概览

简要总结

The purpose of the study is to determine the comparative effectiveness of a provider-only intervention and a parent plus provider intervention to increase initiation of HPV vaccination among male and female patients ages 11-17 in a large pediatric clinic network in the greater Houston area. The hypothesis is that HPV vaccine initiation will be higher in clinics randomized to the parent plus provider intervention compared with clinics randomized to the provider-only intervention.

研究设计

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

入排标准

年龄范围
11 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Patient at a Texas Children's Pediatrics clinic
  • Patient had not initiated the HPV vaccination series at baseline

排除标准

  • Patient had completed the HPV vaccination series at baseline

结局指标

主要结局

Change in percent of HPV vaccination initiation

时间窗: baseline, 3 years

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sally Vernon

◦Blair Justice, PhD Professorship in Mind-Body Medicine and Public Health and Director, Division of Health Promotion and Behavioral Sciences

The University of Texas Health Science Center, Houston

研究点 (2)

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