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NCT05978128NARecruitingAccepts Healthy Volunteers

Utilizing Advocates and Supporters to Increase Lung Cancer Screening Rates in Eligible Participants

Jonsson Comprehensive Cancer Center

Start Date

7/28/2023

Completion Date

9/30/2029

Summary

This clinical trial assesses the use of advocates and supporters of breast and lung cancer screening to increase lung cancer screening rates amongst eligible participants. Imaging-based cancer screening is utilized with variable frequency. Breast cancer screening with mammography has been widely accepted and is commonly used among eligible women. Lung screening with computed tomography scans is poorly used, despite the potential to decrease deaths from lung cancer. There are many reasons lung screening isn't being used when compared to breast screening, such as smoking stigma and fear, along with a lack of awareness of lung screening. By conducting this trial, researchers want to assess the effectiveness of advocates and supporters of breast and lung screening, and to learn about the psychological barriers to cancer screening, identifying those that are unique to lung screening.

Detailed Description

PRIMARY OBJECTIVES: I. Determine the number of patients undergoing breast screening who are eligible to participate in lung screening. II. Determine whether patients currently participating in cancer screening (breast OR lung) are successful as "cancer screening advocates." III. Determine whether laypersons who are aware of screening (including those who accompany friends and family members to their screening appointments) are successful as "cancer screening advocates." IV. Identify knowledge base and psychological barriers to screening through surveys of potential screening participants. OUTLINE: Participants access an electronic patient portal with educational materials at baseline, 1- and 2-year follow-ups, and also interact with a patient navigator on study. Patients also receive materials to share with their friends/family on benefits of breast and lung cancer screening on study. After completion of study intervention, participants are followed up yearly for up to 3 years.

Eligibility Criteria

Age Range: 40 years to 80 years

Inclusion Criteria: * Age: * Breast screening \> 40 * Lung screening 50-80 * Male (M) or Female (F) * Current, former, or never smokers * Close family or friend with smoking history (in or out of state) Exclusion Criteria: * Age: * Breast screening \< 40 * Lung screening \< 50 or \> 80 * Persons who had previously received a diagnosis of lung cancer, had hemoptysis, or had an unexplained weight loss of more than 6.8 kg (15 lb) in the preceding year will also be excluded * Persons with an active cancer

Interventions

BEHAVIORAL

Health Education

OTHER

Health Promotion and Education

BEHAVIORAL

Patient Navigation

OTHER

Survey Administration

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Conditions

Breast CarcinomaLung Carcinoma

Locations

UCLA / Jonsson Comprehensive Cancer Center

Los Angeles, California 90095

United States