RecruitingNot applicableNCT07716280
Official study title

Digital Health Implementation Strategies to Improve Lung Cancer Screening Among Safety-Net Clinics

Study summary

The long-term goal of this program of research is to increase the reach of Lung Cancer Screening (LCS) among low-resource healthcare settings and populations. The proposed project, LUNG-IS, is a mixed-methods, pre-post quasi-experimental design conducted in three Utah safety-net healthcare system clinics. LUNG-IS employs a comprehensive conceptual model with theories, models, and frameworks of implementation and behavioral science, uses rigorous mixed-methods to evaluate factors that influence implementation of LCS, and uses patient navigation to facilitate clinic-community linkages. LUNG-IS leverages existing pathways to care and Centralized Hub infrastructure that enables eligibility assessment, LCS Shared Decision Making (SDM) with clinical decision support, screening referral, and screening logistics assistance to help overcome barriers to LCS completion. The Centralized Hub model uses ubiquitous technologies (i.e., text messaging/telehealth) to enable patients to be assessed for LCS eligibility, engage in SDM if eligible, and be referred for LCS. For patients who decide to complete LCS, they will be provided patient navigation via Community Health Workers designed to address logistical barriers, hesitancy, and financial constraints around completing LCS.

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Key things to know

Main goalPrevention

This describes the study’s primary purpose.

What is being studiedText Messages (TM+) and Chat bot (CA)

Plus 3 other study approaches.

Who it may be forLung Cancer

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Jul 21, 2026 · Source: ClinicalTrials.gov

Is enrollment open?Recruiting

The study is currently accepting participants.

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 Utah

Study sponsor

01
Study overview

What this study is about

Purpose
Prevention
Study type
Interventional
Phase
Not applicable
Sponsor
University of Utah
Interventions being studied
Behavioral: Text Messages (TM+); Behavioral: Chat bot (CA); Behavioral: Video; Behavioral: Reactive Patient Navigation (RPN); Behavioral: Proactive Patient Navigation (PPN)
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
  • Current or former, male and female, smokers.
  • Age 50-80.
  • Primary language English or Spanish.
  • Have a phone that can send/receive text messages.
Reasons someone may not be able to joinExclusion criteria
  • Patients who have never smoked.
  • Patients who are under the age of 50 or above the age of 80.
  • Primary language other than English or Spanish.
  • Do not have access to a phone that can send/receive text messages.

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

  • Huntsman Cancer Institute/ University of UtahSalt Lake City, Utah

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jul 21, 2026. Always confirm current availability with the study team.

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