Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT06898333

Implementation and Effectiveness of the BJC-Pink and Pearl Project on Lung Cancer Screening

Led by Washington University School of Medicine · Updated on 2026-03-25

279

Participants Needed

1

Research Sites

107 weeks

Total Duration

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AI-Summary

What this Trial Is About

The investigators proposal is ripe for executing as the investigators seek to leverage this "natural experiment" initiated by the BJC health system to evaluate the effectiveness of the Pink \& Pearl Campaign as an implementation strategy to promote lung cancer screening (LCS) uptake among LCS-eligible women undergoing mammography at BJC West County. This evaluation is grounded in the Integrated Screening Action Model that depicts individual- and environmental-level influences on the screening behavior process. Using an explanatory sequential mixed methods design, which combines both quantitative and qualitative approaches, the research questions and specific aims for this proposal are to: a) evaluate the baseline prevalence of LCS among LCS-eligible women; b) assess whether the Pink \& Pearl Campaign increases referrals and uptake/ completion of LCS among LCS-eligible women undergoing screening mammography; and c) evaluate individual and environmental factors influencing LCS uptake, and implementation outcomes of the campaign. These implementation outcomes will help identify whether the campaign was put in place successfully or not. This proposal will inform strategies for integrating cancer screening programs to improve poorly performing programs like LCS.

CONDITIONS

Official Title

Implementation and Effectiveness of the BJC-Pink and Pearl Project on Lung Cancer Screening

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Undergoing screening mammography
  • Between the ages of 50 and 80 years (inclusive)
  • Have a 20 pack-year smoking history or quit within the past 15 years
  • Can speak and understand English
  • Able to understand and willing to provide informed consent
Not Eligible

You will not qualify if you...

  • Diagnosed with a serious health problem likely to limit life expectancy (e.g., previous lung cancer)
  • Having symptoms of lung cancer such as coughing up blood or unexplained weight loss over 6.8 kg (15 lb) in the past year
  • Unable or unwilling to receive treatment if lung cancer is found

AI-Screening

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Trial Site Locations

Total: 1 location

1

Barnes-Jewish Hospital West County

Creve Coeur, Missouri, United States, 63141

Actively Recruiting

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Research Team

B

Beryne Odeny, M.D., MPH, Ph.D.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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