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NCT04848961 Clinical Trial

A Study to Develop a Strategy to Increase Lung Cancer Screening in Women Who May Be at Risk for Lung Cancer

Smoking Clinical Trial

Official title:
Leveraging Mammography to Identify and Engage Women at Risk for Lung Cancer in Lung Cancer Screening

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT04848961
Other study ID # 21-103
Secondary ID
Status Active, not recruiting
Phase Early Phase 1
First received
Last updated
Start date April 9, 2021
Est. completion date April 9, 2025

Study information
Verified date May 2024
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to develop a digital strategy to increase awareness about lung cancer screening among women who are eligible to receive it. The digital strategy involves email communications and LungTalk, a web-based (accessed through the Internet) health communication tool that uses text, audio, video, and animation to increase awareness and knowledge about lung cancer screening. This study will focus on women who have recently received a screening mammogram.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 30
Est. completion date April 9, 2025
Est. primary completion date April 9, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria: - LDCT screening-eligible women who received a BiRADS 1 (negative) or 2 (benign/non-cancerous finding) result from a screening mammogram in the last 7 days - Age 50-80 years - = 20-pack-year smoking history of combustible cigarettes as per self report - Women who currently smoke or quit within past 15 years as per self report - Lung screening naïve as per self-report Exclusion Criteria: - Lung cancer diagnosis - Chest CT within the last 12 months

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• LungTalk
MSK developed LungTalk, a novel computer-tailored health communication and decision support tool to (1) increase awareness and knowledge about lung screening; (2) decrease perceived barriers to screening based upon misinformation; and (3) increase screening rates.

Locations
Country Name City State
United States Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities) Basking Ridge New Jersey
United States Memorial Sloan Kettering Cancer Center @ Suffolk-Commack (Limited protocol activity) Commack New York
United States Memorial Sloan Kettering Westchester (Limited Protocol Activities) Harrison New York
United States Hartford Healthcare Cancer Institute @ Hartford Hospital Hartford Connecticut
United States Memorial Sloan Kettering Monmouth (Limited Protocol Activities) Middletown New Jersey
United States Memorial Sloan Kettering Bergen (Limited Protocol Activities) Montvale New Jersey
United States Memorial Sloan Kettering Cancer Center New York New York
United States Memorial Sloan Kettering Nassau (Limited Protocol Activities) Uniondale New York

Sponsors (1)
Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of participants accrued through digital outreach to identify breast screening participants eligible for lung screening Develop a proactive digital outreach and engagement strategy to identify breast screening patients who are eligible for lung screening. 6 months
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