Lung Cancer Clinical Trial

The SHARED, Project, Lung Cancer Screening for African American Men (AAM)

Summary

This study is a single-arm pre-test post-test design with a two-month follow-up assessment. The study aims to provide support to participants in quitting smoking and accessing lung cancer screening through the combination of education interventions and patient navigation (PN)

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Full Description

This study is a single-arm pre-test post-test design with a two-month follow-up assessment. The study aims to provide support to participants in quitting smoking and accessing lung cancer screening through the combination of education interventions and patient navigation (PN). After participant consent the study team will administer a series of surveys to collect the participant's contact information and complete the study's pretest measures. These include a demographic survey, smoking history, lung cancer knowledge, lung screening knowledge, intention to quit/screen, informed to decide, satisfaction survey, and decision conflict survey. The study also consists of three scheduled meetings with the PN lasting up to 60 minutes. The 1st session will be held between 7-14 days after consent. The 2nd session will be held 7-14 after the 1st session and the 3rd session will be held 42-49 days after the 1st session. Additional phone calls will last 10 minutes or less and be focused on specific questions generated by study participants.

In the 1st session the PN will re-orient participant to the goals and objectives of the project and answer participant questions before starting the intervention. The 1st activity will be to show a 3 minute culturally tailored video that will explain the benefits of lung cancer screening for African American Males (AAM) using an internet-enabled device. After completion of the video, the PN will invite the participant to ask any questions that they have and the PN will offer clarifying information. The PN will review with the participant a culturally adapted shared decision-making tool. The participant will complete the posttest surveys as described abov.

In the 2nd session the PN will determine the scheduling and completion of lung cancer screening and Illinois Tobacco Quit Line (ITQL) engagement. The participant will complete the LDCT screening, navigation needs, Quitline Engagement, and decision change surveys

In the 3rd session the PN will determine scheduling, barriers and completion of lung cancer screening and Quitline engagement. The participant will complete LDCT screening check, and a Quitline engagement check

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Eligibility Criteria

Inclusion Criteria:

Self-identify as African American or Black males
Current smokers of any nicotine-containing products
Do not self-report a history of lung cancer symptoms
Speaks English

Exclusion Criteria:

Do not self-identify as African American males
Former smokers
Self-report a history of lung cancer symptoms
Do not speak English

Study is for people with:

Lung Cancer

Estimated Enrollment:

40

Study ID:

NCT05920850

Recruitment Status:

Active, not recruiting

Sponsor:

University of Illinois at Chicago

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There is 1 Location for this study

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University of Illinois
Chicago Illinois, 60612, United States

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Study is for people with:

Lung Cancer

Estimated Enrollment:

40

Study ID:

NCT05920850

Recruitment Status:

Active, not recruiting

Sponsor:


University of Illinois at Chicago

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