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临床试验/NCT06626321
NCT06626321已完成不适用

BE IMMUNE: Behavioral Economics to IMprove and Motivate Vaccination Using Nudges Through the EHR, A Replication Trial

University of Pennsylvania2 个研究点 分布在 1 个国家目标入组 26,248 人开始时间: 2024年10月21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
26,248
试验地点
2
主要终点
Proportion of patients who receive the flu vaccine at the visit

研究概览

简要总结

This study will be a 6-month, cluster randomized, pragmatic replication trial to evaluate the effectiveness of personalized nudges to clinicians and patients, relative to a control, to increase flu vaccination rates among older adults in accordance with CDC guidelines. This will include clinician and patient level nudge interventions, with additional, intensified nudge interventions for patients identified as high risk for not receiving a flu vaccine. Among the intervention clinics, patients will receive pre-visit text message reminders about the flu vaccine, and clinicians will receive a default pended order in the visit encounter in the EHR, along with monthly peer comparison feedback about their flu vaccine completion rate. Patients identified as high risk for noncompletion will be individually randomized to receive an additional bidirectional text message nudge or the standard text messaging

详细描述

Many older adults are at risk of illness, hospitalization, and death from vaccine-preventable diseases. More than half of older adults in the United States are not vaccinated for flu which has remained relatively constant over the past decade, and there are racial, ethnic, and socioeconomic disparities in care. In this study, we will evaluate personalized nudges to clinicians and patients to help increase flu vaccination rates during primary care visits among older adults at three distinct health systems, with a particular focus on population subgroups at high risk for vaccine noncompletion. In a partnership between Penn Medicine and University of Washington (UW) Medicine, a 6-month, multisite, cluster randomized, pragmatic trial with an additional intensification arm for high-risk patients was conducted from September 2023-February 2024. We will now conduct a 6-month replication trial at Lancaster General Health for the 2024-2025 flu season.

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
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients must meet the following criteria to be eligible:
  • Age ≥ 50 years
  • A scheduled new or return (non-urgent/sick) primary care appointment at one of the study practices at Lancaster General Health
  • Have not received their annual flu vaccine during the active intervention period (September- February)
  • Eligible to receive the flu vaccine
  • For the patient intensification nudge, at least one of the following criteria must be met to be considered high risk and randomized to receive the intensification nudge:
  • Age ≥ 70 years
  • Living in a lower income community (lowest quartile, zip-code based)
  • Did not receive a flu vaccine in the previous calendar year
  • Self-identifies as Non-Hispanic Black
  • Clinicians must meet the following criteria to be eligible to receive peer comparison feedback:
  • Practicing physician (MD, DO) or advanced practice provider (NP, PA) with the exception of residents and fellows
  • Have a minimum patient panel of at least 50 patients, and
  • Practicing at a clinical site randomized to receive the clinic-level nudge interventions.

排除标准

  • Patients will be excluded from the study if they:
  • Have a documented allergy to flu vaccine
  • Have a flu vaccine exclusion modifier in Health Maintenance
  • Have opted out of research according to individual site guidelines and policies
  • Have no phone number (home or mobile) listed in their chart

结局指标

主要结局

Proportion of patients who receive the flu vaccine at the visit

时间窗: 4 days from enrollment, at the eligible visit

The primary outcome is flu vaccination completion during the first eligible primary care visit.

次要结局

  • Proportion of patients who receive the flu vaccine within 3 months after the visit(3 months)

研究者

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

Shivan J Mehta

Associate Chief Innovation Officer, Associate Professor of Medicine

University of Pennsylvania

研究点 (2)

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