UCCP21070 / Uptake / Adler
Basic Study Information
Purpose:Location: Strong Hospital
This is a randomized controlled pilot trial of a text-based behavioral intervention
aimed at increasing uptake of lung cancer screening among emergency department patients.
We will conduct a 2-year randomized controlled clinical trial with a prospectively
collected convenience sample of 366 adults who are eligible for LCS but non-adherent
with LCS screening guidelines. Adults aged 50-80 will be recruited from a high-volume
urban ED and a low-volume rural ED, assigned to study conditions, and followed-up
at 150 days to assess interval engagement with the University of Rochester Medical
Center's LCS screening program (primary outcome). Electronic Health Record (EHR) review
will be conducted to assess screening results and subsequent clinical endpoints.
Lead Researcher (Principal Investigator)
Study Contact Information
Study Contact: Clinical Trials Office
Study Location: Wilmot Cancer Institute, University of Rochester Medical Center
Study Email: WCICTOResearch@urmc.rochester.edu
Additional Study Details
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