Skip to content

Enhancing Lung Cancer Screening Through Human-Centered Intervention

Enhancing Lung Cancer Screening Through Human-Centered Intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06351085
Acronym
ELFE
Enrollment
2869
Registered
2024-04-08
Start date
2022-11-10
Completion date
2026-12-31
Last updated
2026-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

Lung Cancer Screening

Brief summary

The purpose of this study is to further understand the factors involved in increasing lung cancer screening.

Detailed description

The study aims to identify patient, primary care team and health system factors that facilitate participation in lung cancer screening. Additionally, conduct a two-arm randomized comparative effectiveness intervention study to increase lung cancer screening compared with a usual care control arm and further evaluate the differential impact of the intervention conditions compared to usual care.

Interventions

BEHAVIORALPre-Visit Planner

The study is comparing the implementation of a Pre-Visit Planner to go through the shared decision making process.

BEHAVIORALPre-Visit Planner + MyChart

The study is comparing the implementation of a Pre-Visit Planner to go through the shared decision making process as well as testing if watching educational videos about the Lung Cancer Screening (LCS) process prior to talking to an LVN will help with LCS uptake.

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
SINGLE (Subject)

Masking description

Biostatistician created a randomized table to allocate patient in either intervention 1 or 2.

Intervention model description

Patients of the intervention clinics will be assigned one of two interventions: 1) Pre Visit Planner (PVP) or 2) PVP + patient education delivered via the MyUCDHealth patient web portal.

Eligibility

Sex/Gender
ALL
Age
50 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

Interviews: * UC Davis Health Systems (UCDHS) primary care providers and clinic staff who provide services to patients ages 50-80. * Patients who are eligible for lung cancer screening. Screening Intervention: \- Patients ages 50-80 who have a history of smoking per review of their electronic medical record and who receive care at the following UCDH ambulatory care clinics: Ellison Ambulatory Care Clinic; Elk Grove; Midtown.

Exclusion criteria

Interviews: * Non-consenting patients and patients who do not speak English or Spanish * Patients aged 49 and younger * Non UCDHS primary care providers and clinic staff Screening Intervention: * UCDHS patients who have already received Lung Cancer Screening * Patients with existing Cancer diagnosis

Design outcomes

Primary

MeasureTime frameDescription
Lung Cancer Screening156 WeeksThe primary outcome is the proportion of patients aged 50-80 with a history of smoking who receive Lung Cancer Screening during the study period; this outcome will be measured in both intervention groups and the control group.

Secondary

MeasureTime frameDescription
Completion of Interviews with Staff and Patients156 WeeksKey informant interviews with UC Davis staff and patients to determine approach to intervention.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026