About this trial
The goal of this clinical trial is to promote lung cancer screening (LCS) uptake among Hispanic current and former smokers. The main questions it aims to answer are:
* What barriers do current and former Hispanic smokers face in the identification and documentation of their smoking status? * How can digital delivery of an educational video promote LCS uptake among current and former Hispanic smokers?
Participants will receive an educational video about lung cancer screening and complete brief, self-reported surveys afterwards.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Must be 50-80 years old
Are a current or former smoker (quit within 15 years, or a cumulative smoking status of > 20 pack-years)
Not currently enrolled in Lung Cancer Screening
Must speak English or Spanish
Disqualifiers
Has a clinical cognitive inability to provide informed consent for participation in the study or complete a brief survey
Currently diagnosed with lung cancer
Currently enrolled in lung cancer screening
Have participated in the focus groups discussions from Aim 1
Trial population
Investigators chose to restrict eligibility to adults aged 50-80 with no personal history of lung cancer to meet the United States Preventive Services Task Force Guidelines for lung cancer screening. As the primary aim of this study is to address the disparities in lung cancer screening rates and outcomes for Hispanic individuals, only Hispanic-identifying patients will be eligible for participation. Further grants stemming from this project will include community-based outreach efforts to extend the testing and dissemination of this intervention to other underrepresented groups.
Trial design
Cohort
Prospective
Treatments tested in this trial
Educational Lung Cancer Screening (LCS) Video
Other interventionAn educational video on lung cancer screening tailored to Hispanic current and former smokers.
Treatment groups
Trial outcomes
Primary outcomes
Participant outreach (contact) of digital link
Reach is defined as \>20% of enrolled participants interacting with the digital delivery of the LCS educational video (i.e., partial or complete review of the LCS educational video).
Secondary outcomes
Participant interaction with digital link
Overall proportion of participants that click on the embedded link to the successfully digitally delivered LCS educational videos
Participant attention of LCS video
Duration of viewing the LCS video (i.e., partial or complete)
Survey completion
Overall proportion of survey completion by participants.
Other outcomes
Participant baseline smoking status
Identify salient participant characteristics obtained from the EHR (e.g., smoking status) among those that interacted with the digital delivery modality.
Participant acceptability of intervention
Investigate attributes of the intervention to guide future research and development to create such an intervention (for future trials)
Sponsors and contacts
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Massachusetts General Hospital
Lead sponsor
National Cancer Institute (NCI)
Collaborator