Building on Trust: Navigating Preventive Lung, Breast, and Prostate Cancer Screenings at Community Resource Spots
Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Observational
SUMMARY
To evaluate a community-based outreach initiative for screening, diagnosis, and treatment of breast, lung, and prostate cancers in underserved adults using the Reach, Effectiveness, Adoption, Implementation, Maintenance (RE-AIM) implementation science framework.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:
• Adult aged 18 or older
• Seeking care at a CRS or emergency department
• Meets criteria for lung, breast, and/or prostate cancer screening, as outlined below:
‣ Lung cancer: Adults aged 50 to 80 years who have a 20 pack-year smoking history and currently smoke or have quit within the past 15 years
⁃ Breast cancer: Women aged 40 to 74 years
⁃ Prostate cancer: Men aged 55 to 69 years
• Receives a positive screening result for lung, breast, and/or prostate cancer at a study site
Locations
United States
Florida
Adventhealth
RECRUITING
Orlando
Contact Information
Primary
Patricia Robinson, PhD
patricia.robinson@adventhealth.com
407-303-3286
Time Frame
Start Date:2025-11-17
Estimated Completion Date:2026-08-31
Participants
Target number of participants:200
Treatments
community-based initiative for screening, diagnosis, and treatment of breast, lung, and prostate
Identify differences between adults who accept or decline cancer follow-up diagnosis and treatment, and clinical trial screening Identify barriers and facilitators to cancer screening, diagnosis, treatment, and clinical trial screening Understand perceptions towards navigators in the cancer care continuum
Recruitment of Stakeholder
Investigators will establish relationships with community stakeholders, providers, and other key personnel to inform them of the program, the study, and opportunities to engage in stakeholder focus groups to provide feedback about program operations. For those interested in participating, a study team member will explain the study and the requirements for participation, review the informed consent form in detail, and obtain consent.