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临床试验/NCT04952376
NCT04952376已完成不适用

Enabling Equitable Access to COVID-19 Vaccine in Under-Resourced Communities

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 1,722 人开始时间: 2021年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
1,722
试验地点
2
主要终点
Dose 1 COVID-19 Vaccine

研究概览

简要总结

This study will deploy a multimodal pragmatic intervention to improve vaccine uptake in priority populations and address vaccine hesitancy to improve access by using a proactive organized population-based outreach leveraging health information technology with tailored navigation support to address mistrust and social barriers.

详细描述

This study will deploy a multimodal pragmatic intervention to improve vaccine uptake in priority populations through a proactive organized population-based outreach approach. It will leverage health information technology with tailored navigation support to address mistrust and social barriers. Study key objectives are to:

  1. conduct a survey of patients to assess and track barriers, intent, and sources of information on COVID vaccine over time.

  2. Determine whether a primary care physician (PCP) endorsement with or without interactive digital communication plus navigation is more effective in promoting uptake of COVID-19 vaccine than general messages from the clinic. Patients will be randomized to one of three arms:

  3. Arm 1: Message about vaccine availability delivered by SMS advising patients to make an appointment.

  4. Arm 2: Same as Arm 1 but delivered as a personalized message text from the PCP.

  5. Arm 3: Same as Arm 2 plus a interactive 2-way SMS options.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 years and older, receiving care at Adelante Healthcare and not vaccinated or already scheduled for vaccination through the health center's appointment system

排除标准

  • Patient younger than 18 or who have been previously or are selected for vaccination during or prior to the week of study enrollment

结局指标

主要结局

Dose 1 COVID-19 Vaccine

时间窗: 30 days

Primary outcome will be the receipt of the first dose of any of the COVID-19 vaccines with FDA emergency use authorization

次要结局

  • Dose 2 COVID-19 Vaccine(60 days)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Chyke A. Doubeni

Principal Investigator

Mayo Clinic

研究点 (2)

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