Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
Healthy Volunteers
ID07287085

Increasing Lung Cancer Screening Uptake Among Emergency Department Patients

Led by University of Rochester · Updated on 2026-05-04

349

Participants Needed

1

Research Sites

35 weeks

Total Duration

On this page

Sponsors

U

University of Rochester

Lead Sponsor

L

Lung Cancer Research Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to increase lung cancer screening (LCS) among patients visiting the emergency department (ED) who are at high risk due to their smoking history. The study compares two approaches to encourage patients to get screened: a basic referral with written materials and a more active facilitated referral combined with motivational text messages. The goal is to see which method leads to more patients completing their lung cancer screening within 120 days. Participants will be randomly assigned to one of two groups. In the basic referral group, patients receive verbal referral and written information to contact the LCS program and their primary care provider. In the facilitated referral group, the study staff submits a requisition to the LCS program on the patient's behalf during their ED visit, and the program will follow up by phone to discuss screening and schedule a CT scan if appropriate. This group also receives a series of motivational text messages to encourage screening. During the study, 300 eligible participants will be followed for about 120 days to track if they complete lung cancer screening. Researchers will collect participant feedback about barriers and motivators to screening and assess the acceptability of ED-based screening promotion. The study includes follow-up to measure screening uptake and any related care. Participation involves receiving referrals, phone calls, and text messages depending on group assignment, with no masking or placebo use.

CONDITIONS

Brief Title

Increasing Lung Cancer Screening Uptake Among Emergency Department Patients

Who Can Participate

Age: 50Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 50 to 80 years
  • At least 20 pack-year smoking history
  • Current smoker or quit smoking within the past 15 years
  • Able to speak and understand English
  • Current patient in the University of Rochester Medical Center involved Emergency Department
Not Eligible

You will not qualify if you...

  • Non-English speakers
  • Unable to provide consent due to high clinical acuity or cognitive deficit
  • Do not have a text-capable mobile phone or cannot use text messaging
  • Not a patient in the University of Rochester Medical Center involved Emergency Department

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) during Emergency Department visit

Behavioral Intervention

Duration - Up to 4 months during participation

Participants receive either a facilitated referral with text messaging support or a basic referral with written materials to encourage lung cancer screening.

Communication and follow-up occur remotely via phone calls and text messages

Surveillance

Duration - Approximately 4 months from enrollment

Participants are observed for lung cancer screening uptake and any downstream care following the intervention.

Assessment at around 120 days after enrollment

Trial Site Locations

Total: 1 location

1

University of Rochester

Rochester, New York, United States, 14642

Actively Recruiting

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Research Team

P

Peter MacDowell

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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