Menu
Recruiting NCT06360822

Increasing Equity in Lung Cancer Screening

No phase Interventional Lung Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: ED-LCS.
Who it may be relevant to
Registry conditions: Lung Cancer. Basic parameters: 50 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The overall objective of this mixed methods study is to: 1) Refine the Emergency Department Lung Cancer Screening (ED-LCS) intervention using qualitative interviews among key stakeholders; 2) pilot test the ED-LCS intervention evaluating the intervention efficacy, acceptability, and feasibility; and 3) provide an in-depth description of stakeholders' experiences with the ED-LCS intervention for future refinement.

Interventions

  • Behavioral ED-LCS
    This is a lung cancer educational intervention for patients in the emergency department.

Primary outcome measures

  • Rate of patients receive Lung Cancer Screening [Time frame: 6-12 months]
Secondary outcome measures (1)
  • Patients ratings of intervention [Time frame: At delivery]

Eligibility criteria

Inclusion criteria

  • • Eligible for LCS (50-80 years old, smoked in past 15 years, and smoked at least 20 pack years)

Exclusion criteria

  • • Non-English/Spanish speaking
  • Decompensated psychiatric illness (suicidal, homicidal, psychosis). Will confirm with attending physicians at time of enrollment
  • Intoxicated with alcohol or drugs
  • Cannot provide reliable follow up contact information (cell phone)
  • Presenting to the ED with a life-threatening condition
  • Have received chest CT scan in past 12 months
  • Already enrolled in LCS
  • Hospice enrolled

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Health services research

Study locations

United States · 1 center
  • Eskenazi Health — Indianapolis

Identifiers

NCT: NCT06360822 · 19317

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗