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Educating Smokers About Lung Cancer Screening Using Tobacco Quitlines

Educating Smokers About Lung Cancer Screening Using Tobacco Quitlines

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04595422
Enrollment
800
Registered
2020-10-20
Start date
2020-07-02
Completion date
2026-10-31
Last updated
2026-04-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Carcinoma

Brief summary

This implementation study will examine the best ways to refer heavy smokers to information about lung cancer screening.

Detailed description

PRIMARY OBJECTIVE: I. To increase the number of smokers eligible for lung cancer screening (LCS) who receive high-quality educational materials about LCS through tobacco quitlines. OUTLINE: CALL CENTER STAFF: Participants undergo training consisting of a 60-minute educational session. CALLERS SUBSTUDY: Participants are referred to lung cancer screening educational materials. Participants also complete questionnaires at 1 week and 6 months after referral to educational materials.

Interventions

OTHEREducational Intervention

Undergo training consisting of a 60-minute educational session

OTHERQuestionnaire Administration

Complete questionnaire

OTHERSurvey Administration

Ancillary studies

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* QUITLINE CALL CENTER STAFF * Staff member of a quitline * Aged 18 years and above * CALLERS (SMOKERS WHO CONTACT THE QUITLINE ABOUT SMOKING CESSATION SERVICES) INCLUSION CRITERIA * Callers 55-80 years of age * Current smoker, or former smoker with a cessation history of \< 15 years * \>= 30 pack-year smoking history * English-speaking

Exclusion criteria

* CALLERS (SMOKERS WHO CONTACT THE QUITLINE ABOUT SMOKING CESSATION SERVICES)

Design outcomes

Primary

MeasureTime frameDescription
Content from communications (email, phone, monthly calls)Up to 4 yearsWill be content analyzed using Atlas.ti qualitative software according to the adaptation framework from Stirman and colleagues. Will identify 1) who made the modification; 2) what was modified (i.e., content, context, training and evaluation); 3) for whom the modification was made (e.g., individual counselor); 4) context of the modification (e.g., format, setting, personnel, population); and 5) what was the nature of the modification (e.g., adding elements). Will also code for facilitators and barriers that are consistent with the constructs from CFIR. All textual data will be double coded and discussed by the researchers.
Healthcare sector perspectiveUp to 4 yearsAs needed, will use a process-flow analysis to identify all resources utilized at each of the step of the program.
ReachDuring 6 month implementation periodThe analysis of the data from the logs and surveys will include examining the means, medians, standard deviations, and ranges overall and by state quitline for Reach
Overall lung cancer screening rateUp to 6 months
Effectiveness (Caller Substudy)Up to 6 monthsWill be successful if callers who participate in the evaluation answer at least 58 percent (7/12) of the Adapted lung cancer screening (LCS)-12 Knowledge Measure questions correctly and have a PrepDM score of at least 80 (standard deviation \[SD\] = 17.7), which were observed in the original project.

Countries

United States

Contacts

CONTACTRobert J. Volk
bvolk@mdanderson.org713-563-0020
PRINCIPAL_INVESTIGATORRobert J Volk

M.D. Anderson Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 17, 2026