Actively Recruiting

Phase Not Applicable
Age: 50Years - 77Years
All Genders
NCT07322367

A Mobile Patient Health Technology Intervention for Improving Lung Cancer Screening Rates in Eligible High Risk Patients

Led by Wake Forest University Health Sciences · Updated on 2026-03-25

27000

Participants Needed

1

Research Sites

40 weeks

Total Duration

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Sponsors

W

Wake Forest University Health Sciences

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

A Mobile Patient Health Technology Intervention for Improving Lung Cancer Screening Rates in Eligible High Risk Patients

Who Can Participate

Age: 50Years - 77Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 50 to 77 years
  • Smoked at least 20 pack years
  • Current smoker or quit smoking within the past 15 years
  • Established with a primary care provider within the Atrium Health Wake Forest Baptist health network
  • 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
Not Eligible

You will not qualify if you...

  • Need for a language interpreter other than Spanish
  • Prior history of lung cancer
  • Chest CT within the last 12 months
  • Meeting HEDIS COL-E measure exclusion criteria due to significant comorbidities or frailty

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Atrium Health Wake Forest Baptist

Winston-Salem, North Carolina, United States, 27157

Actively Recruiting

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Research Team

S

Study Coordinator

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

4

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