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N/A N=1,094 Randomized Health Services Research

Implementation of Smoking Cessation Within NCI Community Oncology Research Program (NCORP) Sites

Smoking Cessation

Enrolled (actual)
1,094
Serious AEs
Results posted
Jul 2022
Primary outcome: Primary: Percentage of Patients With 7-day Sustained Smoking Abstinence Reported in the Patient Survey — 13.0; 13.5 percentage of participants — p=0.865

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Personnel Training and Coaching Calls (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Wake Forest University Health Sciences
Primary completion
Feb 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Patients With 7-day Sustained Smoking Abstinence Reported in the Patient Survey
13.0; 13.5 0.865
SECONDARY
Salivary Cotinine Test for Non-Smokers
13; 10; 10; 20; 28; 31
SECONDARY
Short-term Smoking Abstinence - Patient Survey
6.5; 5.5
SECONDARY
Total Number of Services Participant Reported Received at 14 Days
7.51; 7.86

Summary

Evaluate a multi-faceted training program to improve short-term smoking cessation rates (<14 days post-visit) and short (3 months) and sustained abstinence (6 months) among 1,114 enrolled smokers who present for low-dose computed tomography (LDCT) lung cancer screening in 26 community-based practices.

Eligibility Criteria

Inclusion Criteria

  • Agrees to have NCORP research personnel serve as the study liaison and another person to serve as the cessation program champion.
  • Agrees to participate in all aspects of the intervention, randomization, and evaluation.
  • Agrees to participate in a confidential 1-on-1 semi-structured interview with the research team.
  • Agrees to have the interview taped, transcribed and qualitatively analyzed.
  • Age ≥18 years
  • Potential participants will be screened using the following question: "Do you smoke cigarettes every day, some days, or not at all?" (BRFSS). A current smoker is anyone responds "every day" or "some days".

Exclusion Criteria

  • Current use (previous 30 days) of a tobacco dependence treatment including bupropion, varenicline, and nicotine replacement
  • Individuals who use e-cigarettes and who are not smoking cigarettes. Dual users (those who use both e-cigarettes and cigarettes) will still be included in the trial.
  • The presence of a physical or cognitive impairment that would prevent a person from engaging in survey research (such as blindness, deafness, or dementia).
  • Individual has already completed the intended LDCT lung cancer screening for this study.
  • Non-English speaking participants.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03291587). 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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