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Clinical Trials/NCT06909981
NCT06909981Not yet recruitingNot Applicable

Community-Based Engagement to Improve Lung Cancer Screening and Outcomes

Brigham and Women's Hospital0 sites125 target enrollmentStarted: May 1, 2026Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
125
Primary Endpoint
Feasibility of mobile lung cancer screening in target communities in Boston, Massachusetts.

Study Overview

Brief Summary

The main goal of this pilot study is to understand the impact of a mobile lung cancer screening clinics in individuals from neighborhoods and communities with less access to resources in Boston, Massachusetts who are at high risk for lung cancer. A secondary goal of this pilot study is to understand how social determinants of health impact these neighborhoods and communities. Another secondary goal of this pilot study is to see if video recording of participants speaking to their future selves and sending the videos back to participants to encourage them to get lung cancer screening after one year can be administered in a mobile lung cancer screening setting. The questions this study aims to answer are:

  • Is mobile lung cancer screening is feasible and acceptable?
  • Is collecting social needs data during the mobile lung cancer screening clinics feasible?
  • Is creating video recordings of patients encouraging their future selves to get lung cancer screening after one year feasible?

Participants will:

  • Complete an intake survey, providing information about their demographic, medical, and social needs information.
  • Undergo a shared decision-making conversation to determine whether lung cancer screening should be done.
  • Undergo lung cancer screening.
  • Undergo a debriefing conversation and fill out an acceptability survey.
  • Record a video speaking to their future selves about the importance of annual lung cancer screening, with the video to be sent back to them after roughly one year.
  • Undergo a semi-structured phone interview between four and eight weeks after lung cancer screening date.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
50 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Ability to understand and the willingness to sign a written informed consent document prior to any study-related procedures.
  • Willing to undergo treatment.
  • Adults between the ages of 50 and 80 years.
  • No recent CT imaging within the last year.
  • Currently smokes tobacco or has quit smoking tobacco within the past 15 years.
  • Has a tobacco smoking history of at least 20 pack years (i.e. one pack per day for the last 20 years or equivalent).
  • Has never been diagnosed with lung cancer.

Exclusion Criteria

  • Adults/children less than 50 years, or greater than 80 years of age.
  • Has never smoked tobacco.
  • Has smoked tobacco but quit more than 15 years ago.
  • Has a tobacco smoking history of less than 20 pack years.
  • Presence of major comorbidity(ies) that could prevent treatment.
  • Previous diagnosis of lung cancer.
  • In the opinion of the investigator, the subject is not an appropriate candidate for the study.

Outcomes

Primary Outcomes

Feasibility of mobile lung cancer screening in target communities in Boston, Massachusetts.

Time Frame: During the intervention.

This outcome will be assessed by calculating the raw count of individuals screened at each mobile clinic and the number of individuals unable to be screened due to time constraints.

Acceptability of mobile lung cancer screening in target communities in Boston, Massachusetts.

Time Frame: Between four and eight weeks after the intervention

Acceptability will be assessed using semi-structured phone interviews with participants. Responses to questions, themes, and keywords will be analyzed to report attitudes regarding the intervention.

Secondary Outcomes

  • Feasibility of collecting social determinants of health data during mobile lung cancer screening clinics in underserved communities in Boston, Massachusetts.(Pre-intervention)
  • Feasibility of collecting social determinants of health data during mobile lung cancer screening clinics in underserved communities in Boston, Massachusetts.(Pre-intervention)
  • Feasibility of administering a video-based intervention to encourage annual lung cancer screening(From enrollment until the end of the study.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Rian M. Hasson, MD, MPH, FACS

Associate Surgeon, Vice Chair for Workforce Development & Engagement

Brigham and Women's Hospital

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