N/A
N=1,219
Evaluation of a Scalable Decision Support and Shared Decision Making Tool for Lung Cancer Screening
Early Detection of Cancer · Lung Neoplasms
Bottom Line
View on ClinicalTrials.gov: NCT04498052 ↗Enrolled (actual)
1,219
Serious AEs
0.0%
Results posted
Mar 2025
Primary outcome: Primary: Number of Participants With Lung Cancer Screening (LCS) Care-Gap Closed — 588 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- EHR-integrated Shared Decision Making Tool and Clinical Decision Support for Lung Cancer Screening (Other)
- Age
- Adult, Older Adult · 55+ yrs
- Sex
- All
- Sponsor
- University of Utah
- Primary completion
- Apr 2022
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants With Lung Cancer Screening (LCS) Care-Gap Closed |
588 | — |
Summary
The purpose of this project is to increase appropriate low-dose computed tomography (LDCT) lung cancer screening through the development and wide dissemination of patient-centered clinical decision support (CDS) tools that (1) are integrated with the electronic health record (EHR) and clinical workflows, (2) prompt for shared decision making (SDM) when patients meet screening criteria, and (3) enable effective SDM using individually-tailored information on the potential benefits and harms of screening. The study will promote standard of care that is endorsed by the Centers for Medicare & Medicaid Services (CMS) and the US Preventive Services Task Force (USPSTF).
Eligibility Criteria
Inclusion Criteria
- receives care at University of Utah primary care clinics;
- does not already have lung cancer;
- meets USPSTF criteria for LDCT screening (currently, age >= 55 years and <= 80 years old at the time of the visit; 30+ pack-year smoking history and current smoker or quit in the past 15 years).
Exclusion Criteria
- None
Data sourced from ClinicalTrials.gov (NCT04498052). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.