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Building on Trust: Navigating Preventive Lung, Breast, and Prostate Cancer Screenings at Community Resource Spots

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AdventHealth

Status

Enrolling

Conditions

Breast Cancer
Lung Cancer (Diagnosis)
Prostate Cancer

Treatments

Behavioral: referral for definitive diagnosis based on their cancer screening results
Behavioral: Engagement

Study type

Observational

Funder types

Other

Identifiers

NCT07231159
2343026
333

Details and patient eligibility

About

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.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Adult aged 18 or older

  2. Seeking care at a CRS or emergency department

  3. Meets criteria for lung, breast, and/or prostate cancer screening, as outlined below:

    1. 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
    2. Breast cancer: Women aged 40 to 74 years
    3. Prostate cancer: Men aged 55 to 69 years
  4. Receives a positive screening result for lung, breast, and/or prostate cancer at a study site

Exclusion criteria

  1. Displays behavior disruptive to other patients or staff
  2. Refusal to accept screening for breast, lung, and/or prostate cancers

Trial design

200 participants in 2 patient groups

community-based initiative for screening, diagnosis, and treatment of breast, lung, and prostate
Description:
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
Treatment:
Behavioral: referral for definitive diagnosis based on their cancer screening results
Recruitment of Stakeholder
Description:
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.
Treatment:
Behavioral: Engagement

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Patricia Robinson, PhD

Data sourced from clinicaltrials.gov

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