CompletedNot applicableNCT04979169
Official study title

Emergency Department Lung Cancer URMFG Pilot

Study summary

This is a randomized controlled pilot trial of a text-based behavioral intervention aimed at increasing uptake of lung cancer screening among emergency department patients. We will conduct a 2-year randomized controlled clinical trial with a prospectively collected convenience sample of 366 adults who are eligible for LCS but non-adherent with LCS screening guidelines. Adults aged 50-80 will be recruited from a high-volume urban ED and a low-volume rural ED, assigned to study conditions, and followed-up at 150 days to assess interval engagement with the University of Rochester Medical Center's LCS screening program (primary outcome). Electronic Health Record (EHR) review will be conducted to assess screening results and subsequent clinical endpoints.

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Key things to know

Main goalPrevention

This describes the study’s primary purpose.

What is being studiedText Messaging

The study team can explain what participation involves.

Who it may be forLung Cancer

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Aug 15, 2023 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Interventional

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?University of Rochester

Study sponsor

01
Study overview

What this study is about

Purpose
Prevention
Study type
Interventional
Phase
Not applicable
Sponsor
University of Rochester
Interventions being studied
Behavioral: Text Messaging
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • Age 50 - 80
  • 20+ pack-year smoking history
  • current smoker or quit within 15 years
  • English, ASL, or Spanish speaking
  • Presenting as a patient at the Strong Memorial or Noyes Community Hospital EDs
Reasons someone may not be able to joinExclusion criteria
  • Non-English, Non-Spanish, and Non-ASL speaking
  • Inability to consent (e.g. high clinical acuity)
  • Lack of text-capable mobile phone and/or inability to use text function

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Strong HospitalRochester, New York

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Aug 15, 2023. Always confirm current availability with the study team.

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