Enhancing Lung Cancer Screening Through Human-Centered Intervention

N/AActive Not RecruitingNCT06351085

University of California, Davis2,869 enrolled

Overview

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

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SCREENING

Masking

SINGLE

Enrollment

2,869

Conditions

Lung Cancer

Interventions

Pre-Visit PlannerBEHAVIORAL

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

Pre-Visit Planner + MyChartBEHAVIORAL

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.

Eligibility

Sex: ALLMin age: 50 YearsMax age: 80 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (1)

University of California, Davis

Sacramento, California, United States

Outcomes

Primary Outcomes

Lung Cancer Screening

The 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.

Time frame: 156 Weeks

Secondary Outcomes

Completion of Interviews with Staff and Patients

Key informant interviews with UC Davis staff and patients to determine approach to intervention.

Time frame: 156 Weeks

Data from ClinicalTrials.gov

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