Dissemination Of Lung Cancer Screening Education Through Tobacco Quitlines
2 other identifiers
interventional
650
1 country
1
Brief Summary
The goal of this research study is to compare two different ways to increase lung cancer screening rates for tobacco quitline clients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable lung-cancer
Started Jan 2027
Longer than P75 for not_applicable lung-cancer
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 17, 2026
CompletedFirst Posted
Study publicly available on registry
July 22, 2026
CompletedStudy Start
First participant enrolled
January 1, 2027
ExpectedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2032
Study Completion
Last participant's last visit for all outcomes
June 30, 2034
July 22, 2026
July 1, 2026
5.5 years
July 17, 2026
July 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Safety and Adverse Events (AEs)
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 6.0
Through study completion; an average of 1 year
Study Arms (2)
CMP: Comparator - Low-Touch Strategy (Usual Practice): LCS Educational Resources
EXPERIMENTALInvestigators will use a parallel randomized controlled trial to compare a high-touch strategy (emailing/texting + decision coaching + navigation) to a low-touch strategy (emailing/texting) to distribute evidence based LCS educational resources to increase awareness and demand for LCS among quitline clients.
INT: Intervention - High-Touch Strategy: LCS Educational Resources, Decision Coaching, Navigation
EXPERIMENTALInvestigators will use a parallel randomized controlled trial to compare a high-touch strategy (emailing/texting + decision coaching + navigation) to a low-touch strategy (emailing/texting) to distribute evidence based LCS educational resources to increase awareness and demand for LCS among quitline clients.
Interventions
Participants will receive the LCS educational materials, decision coaching call for the SDM visit, and navigation for LCS.
Eligibility Criteria
You may qualify if:
- Quitline Client
- Quitline client participants must meet the criteria for LCS with regards to age (50 to 80 years) and smoking history (20+ pack-years). This project will not re-confirm quitline client participant eligibility for screening. Tobacco treatment specialists will elicit study interest from only eligible quitline clients.
- Representative of the Quitline Community
- Representative of the Quitline Community will include any employee of the quitline service provider, representative from an organization that collaborates or funds a tobacco quitline, and/or a representative of the state department of health. All individuals will be adults (18 years and older) and able to speak English.
- Representative of the Healthcare Sector
- Representative of the healthcare sector will include any adult who works in healthcare, including but not limited to physicians, healthcare administrative leaders/managers, nurses, advanced practice providers. All individuals will be adults (18 years and older) and able to speak English.
You may not qualify if:
- Not applicable as our focus on quitline clients and representatives (adults) of the quitline community or the healthcare sector.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
UT MD Anderson
Houston, Texas, 77030, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lisa Lowenstein, PHD
UT MD Anderson
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 17, 2026
First Posted
July 22, 2026
Study Start (Estimated)
January 1, 2027
Primary Completion (Estimated)
June 30, 2032
Study Completion (Estimated)
June 30, 2034
Last Updated
July 22, 2026
Record last verified: 2026-07