Evaluating the Implementation and Effectiveness of the Pink and Pearl Campaign on Lung Cancer Screening at Christian Hospital

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20+
SponsorWashington University School of Medicine

About this trial

Inspired by the ongoing Pink \& Pearl Campaign, the breast radiology service of Christian Hospital in north St. Louis County will partner with Siteman Cancer Center to pilot this campaign in its mammography clinics in order to promote awareness, referral, and completion of lung cancer screening (LCS) among eligible women. This campaign leverages established infrastructure such as nurse navigation and referral to screening or primary care for further shared decision-making on cancer screening. The purpose of this study is to evaluate the effectiveness of the Pink \& Pearl Campaign in improving LCS uptake among LCS-eligible women undergoing mammography at Christian Hospital. 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, our specific aims for this proposal are to: a) assess whether the Pink \& Pearl Campaign increases referrals and uptake/completion of LCS among LCS-eligible women undergoing screening mammography; b) determine median time-to-screening after referral to LCS; and c) evaluate individual and health system 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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Undergoing screening mammography at Christian Hospital

Between the ages of 50-80 years (inclusive)

Part of the interventional study

Reporting a 20 pack-year equivalent of either current smoking history or have quit in the past 15 years

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pink and Pearl Campaign

    Other intervention

    This campaign leverages established infrastructure such as nurse navigation and referral to screening or primary care for further shared decision-making on cancer screening.

Treatment groups

5,515 Participants
are divided into 2 treatment groups
Group A: Participants - scheduled for mammography and eligible for LCSExperimental treatment 1 intervention
Group B: ProvidersNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Proportion of women referred from the breast radiology service who successfully complete LCS 6-months post-Pink & Pearl implementation

The investigators will compare the baseline prevalence of LCS among women undergoing BCS to the prevalence of LCS among women undergoing BCS 6 months after implementation of the Pink \& Pearl Campaign.

Time frame
At 6 months

Secondary outcomes

1

Median time-to-screening

The investigators will compare differences in time-to-lung cancer screening across heterogenous populations

Time frame
At 6 months
2

Acceptability of Pink & Pearl Campaign

Defined as the perception that the campaign is agreeable or satisfactory

Time frame
At 6 months

Other outcomes

1

Number of individual level barriers to LCS completion

Time frame
At 6 months
2

Number of health system level barriers to LCS completion

Time frame
At 6 months
3

Feasibility of Pink & Pearl Campaign

Defined as extent to which strategy is suitable for a routine use in a setting

Time frame
At 6 months
4

Appropriateness of Pink & Pearl Campaign

Defined as perceived fit, relevance or compatibility of the strategy or practice for a given setting

Time frame
At 6 months

Sponsors and contacts

Click on the lead sponsor to view all of their trials.