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临床试验/NCT07322367
NCT07322367尚未招募不适用

A Pragmatic Randomized-Controlled Learning Health System Trial

Wake Forest University Health Sciences1 个研究点 分布在 1 个国家目标入组 27,000 人开始时间: 2026年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
27,000
试验地点
1
主要终点
Number of Participants to Complete Lung Screening CT - Primary Effectiveness

研究概览

简要总结

To evaluate the real-world effectiveness and implementation strategies for mPATH-Lung, investigators propose a pragmatic, randomized controlled trial across an academic Learning Health System. The trial will contrast several approaches to participant outreach and will specifically target engaging fully powered cohorts of racial/ethnic minorities and rural residents.

详细描述

Primary Objective: Evaluate the real-world effectiveness of mPATH-Lung in increasing lung cancer screening rates across diverse populations.

Secondary Objectives

  • Compare the differential effectiveness of three outreach strategies for engaging participants with mPATH-Lung across vulnerable rural or ethnic/racial minority population subgroups.
  • Estimate the additional revenue generated by mPATH-Lung through increased screening and downstream care.
  • Evaluate the potential for over-screening and the impact of applying HEDIS-based exclusion criteria

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Screening
盲法
Single (Investigator)

入排标准

年龄范围
50 Years 至 77 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Eligible patients will:
  • Meet the Medicare criteria for lung cancer screening, as updated in February 2022:
  • Age 50 - 77 years
  • Smoked at least 20 pack years
  • Current smoker or quit smoking within the past 15 years
  • Be established with a primary care provider within the Atrium Health Wake Forest Baptist health network (defined as having completed at least 1 primary care appointment in the past 6 months or have completed at least 2 primary care appointments within the past 18 months or being scheduled to see a health network primary care provider within the next 30 days).
  • Have a patient portal account or cellphone number listed in the electronic health record
  • Have a North Carolina address listed in the electronic health record

排除标准

  • The following patients will be excluded:
  • Patients flagged as needing a language interpreter in the electronic health record for any language other than Spanish (electronic messages and intervention are deliverable in English or Spanish only)
  • Those for whom lung cancer screening would be or may be inappropriate:
  • electronic health record Prior history of lung cancer electronic health record Chest CT within the last 12 months electronic health record Those meeting the HEDIS COL-E measure exclusion criteria based on significant comorbidities and/or frailty.

研究组 & 干预措施

Arm A

Experimental

Patient portal message first followed by up to 3 reminder text messages.

干预措施: Portal Message with Reminder Text Messages (Other)

Arm B

Experimental

Text message only with up to 3 reminder text messages.

干预措施: Text Message with Reminder Text Messages (Other)

Arm C

Experimental

Portal message only with no reminder messages.

干预措施: Portal message only (Other)

Usual Care Arm

Active Comparator

Patients receive usual care.

干预措施: Usual Care (Other)

结局指标

主要结局

Number of Participants to Complete Lung Screening CT - Primary Effectiveness

时间窗: 90 days

Completion of the lung screening CT by participants.

次要结局

  • Number of Participants with Eligibility for Lung Screening(90 days)
  • Number of Requests for Lung Screening(90 days)
  • Number of Orders for Lung Screening CT Scans(Within 90 days of randomization)
  • Amount of Revenue Generated(12 months following completion of screenings)
  • Number of Participants that Represent Over-screening(90 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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