Increasing Lung Cancer Screening Uptake Among Emergency Department Patients
Overview
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- University of Rochester
- Enrollment
- 349
- Locations
- 1
- Primary Endpoint
- Assessment for LCS Uptake and Downstream Care
Overview
Brief Summary
The objective of the proposed clinical trial is to determine if we can increase LCS among ED patients using a combination of facilitated referral to an LCS program plus text message reminders to get screened. Step 1 of the approach is to identify participants that are eligible for LCS. Step 2 is to randomize eligible study participants between two study arms: (1) basic referral for LCS (i.e.
verbal referral with written materials), and (2) facilitated referral for LCS (i.e. submission of a requisition to LCS program by staff) plus a subsequent series of text messages aimed at generating intention and motivation to get screened. The investigators' preliminary work showed this approach was feasible in the ED setting. The proposed study will build on this preliminary work with the goal of having a significant positive impact on LCS uptake.
A total of 300 individuals eligible for LCS will be recruited from a high-volume urban ED, randomized between study arms, and followed-up at 120 days to assess interval LCS uptake. The Specific Aims of the proposed project are, (1) Compare LCS uptake between the two study arms, (2) Identify predictors of individuals that are not up-to-date with LCS at the time of enrollment, and (3) Evaluate study participant feedback on (a) barriers and facilitators to getting screened and (b) acceptability and appropriateness of ED-based promotion of LCS. The study team is at the forefront of developing ED-based interventions to promote cancer screening. This project leverages the universal access setting of the ED to identify individuals at greatest risk for lung cancer and get them screened. A scalable ED-based intervention that increases LCS uptake would save lives.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Screening
- Masking
- None
Eligibility Criteria
- Ages
- 50 Years to 80 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Age 50 - 80
- •≥ 20 pack-year smoking history
- •current smoker or quit within 15 years
- •English speaking
- •Current patient in URMC involved Emergency Department
Exclusion Criteria
- •Non-English
- •Inability to provide consent (e.g. high clinical acuity, cognitive deficit)
- •Lack of text-capable mobile phone and/or inability to use text function
- •Not being a patient in URMC involved Emergency Department There are no restrictions for gender, racial and ethnic origins.
Outcomes
Primary Outcomes
Assessment for LCS Uptake and Downstream Care
Time Frame: From enrollment through participation with first assessment at ~ 120 days of participation.
The primary outcome, LCS uptake, will be assessed via telephone follow-up and EHR review.
Secondary Outcomes
No secondary outcomes reported