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N/A N=944 Randomized Treatment

Promoting Smoking Cessation in Lung Cancer Screening Through Proactive Treatment

Smoking Reduction · Tobacco Use · Tobacco Smoking · Tomography · Lung Diseases

Enrolled (actual)
944
Serious AEs
Results posted
Oct 2024
Primary outcome: Primary: Self-reported Smoking Abstinence — 50; 51 Participants — p=0.83

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Unsigned note to provider about cessation medication prescription (Behavioral); Proactive Telephone Counseling from VA Quitline (Behavioral)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Feb 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Self-reported Smoking Abstinence
50; 51 0.83
SECONDARY
Cost of Smoking Cessation Care
34.1; 384.2
SECONDARY
Patients' Experience With Telephone Counseling
34
SECONDARY
Patients' Motivational Assessment
7.48; 7.3
SECONDARY
Patients' Perception of Susceptibility to Harm
1.97; 2.09
SECONDARY
Patients' Self-efficacy Assessment
5.8; 6.1
SECONDARY
Patients' Motivational Assessment
7.48; 7.3
SECONDARY
Patients' Self-efficacy Assessment
5.8; 6.1

Summary

This pragmatic trial will evaluate the value of routinely providing proactive smoking cessation support to current smokers as a part of participating in lung cancer screening within Veterans Health Administration.

Eligibility Criteria

Inclusion Criteria

  • Providers who schedule patients for a lung cancer screening at either of the two VA sites.
  • Patients who participate in lung cancer screening and are current smokers at the time of scheduling their screening exam.

Exclusion Criteria

  • Providers who currently systematically prescribe cessation support medication to all current smokers will be excluded.
  • Patients with urgent findings requiring biopsy/immediate attention on the screening CT will be excluded.
  • Patients with a prior diagnosis of lung cancer or who are receiving active therapy for any cancer, except skin cancer, will be excluded.
  • Patients previously diagnosed with cognitive impairment, dementia, or severe behavioral disorders, or have an indication in chart review of difficulty communicating or participating in telephone counseling sessions will be excluded.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03612804). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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