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Recruiting NCT04595422

Educating Smokers About Lung Cancer Screening Using Tobacco Quitlines

No phase Interventional Lung Carcinoma

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: Educational Intervention, Educational Intervention, Questionnaire Administration, Survey Administration.
Who it may be relevant to
Registry conditions: Lung Carcinoma. Basic parameters: from 18 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 →

Unsure about the terms? Read our patient guide →

Overview

This implementation study will examine the best ways to refer heavy smokers to information about lung cancer screening.

Detailed description

PRIMARY OBJECTIVE:

I. To increase the number of smokers eligible for lung cancer screening (LCS) who receive high-quality educational materials about LCS through tobacco quitlines.

OUTLINE:

CALL CENTER STAFF: Participants undergo training consisting of a 60-minute educational session.

CALLERS SUBSTUDY: Participants are referred to lung cancer screening educational materials. Participants also complete questionnaires at 1 week and 6 months after referral to educational materials.

Interventions

  • Other Educational Intervention
    Undergo training consisting of a 60-minute educational session
  • Other Educational Intervention
    Receive lung cancer screening educational materials
  • Other Questionnaire Administration
    Complete questionnaire
  • Other Survey Administration
    Ancillary studies

Primary outcome measures

  • Content from communications (email, phone, monthly calls) [Time frame: Up to 4 years]
  • Healthcare sector perspective [Time frame: Up to 4 years]
  • Reach [Time frame: During 6 month implementation period]
  • Overall lung cancer screening rate [Time frame: Up to 6 months]
  • Effectiveness (Caller Substudy) [Time frame: Up to 6 months]

Eligibility criteria

Inclusion criteria

  • QUITLINE CALL CENTER STAFF
  • Staff member of a quitline
  • Aged 18 years and above
  • CALLERS (SMOKERS WHO CONTACT THE QUITLINE ABOUT SMOKING CESSATION SERVICES) INCLUSION CRITERIA
  • Callers 55-80 years of age
  • Current smoker, or former smoker with a cessation history of < 15 years
  • >= 30 pack-year smoking history
  • English-speaking

Exclusion criteria

  • CALLERS (SMOKERS WHO CONTACT THE QUITLINE ABOUT SMOKING CESSATION SERVICES) EXCLUSION CRITERIA
  • History of lung cancer by self-report

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

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Sequential
Masking
Open label
Primary purpose
Health services research

Study locations

United States · 1 center
  • M D Anderson Cancer Center — Houston

Identifiers

NCT: NCT04595422 · 2020-0013 · NCI-2020-03812 · 2020-0013

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗