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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05920850
Other study ID # 2023-0273
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date July 14, 2023
Est. completion date August 31, 2024

Study information

Verified date May 2024
Source University of Illinois at Chicago
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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)


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


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 40
Est. completion date August 31, 2024
Est. primary completion date August 31, 2024
Accepts healthy volunteers No
Gender Male
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria: 1. Self-identify as African American or Black males 2. Current smokers of any nicotine-containing products 3. Do not self-report a history of lung cancer symptoms 4. Speaks English Exclusion Criteria: 1. Do not self-identify as African American males 2. Former smokers 3. Self-report a history of lung cancer symptoms 4. Do not speak English

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Educational Video about LDCT lung cancer screening
A culturally tailored video that provides education about the process LDCT lung cancer screening
A culturally tailored shared decision-making tool
A culturally tailored shared decision-making tool that educates participants about the shared decision-making process
Flip chart
The use of a flip chart that reinforces the information provided in the video and shared decision-making tool
Navigation support
Navigation support for participants who express interest in LDCT and quitting smoking.

Locations

Country Name City State
United States University of Illinois Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
University of Illinois at Chicago

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assess changes in knowledge, attitudes, risk perception, and intention/ stage of readiness to engage in lung cancer screening and smoking cessation Number of participants that show an improvement from pretest to poattest 1 year
Primary Assess the completion of a healthcare visit for the purpose of lung cancer screening ces Number of participants that complete lung cancer screeninf 1 year
Primary Assess completion of referral to smoking cessation treatment Number of participants that completed the referral to smoking cessation treatment to the ITQL 1 year
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