Implementation of Smoking Cessation Within NCI Community Oncology Research Program (NCORP) Sites
(OaSiS Trial)
Recruiting in Palo Alto (17 mi)
+48 other locations
Age: 18+
Sex: Any
Travel: May Be Covered
Time Reimbursement: Varies
Trial Phase: Academic
Waitlist Available
Sponsor: Wake Forest University Health Sciences
No Placebo Group
Approved in 6 Jurisdictions
Trial Summary
What is the purpose of this trial?
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.
See 3 more
Treatment Details
Interventions
- Smoking Cessation (Behavioural Intervention)
Participant Groups
2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment1 Intervention
Training of Lung Cancer Screening Personnel on implementation of the United States Public Health Service (US PHS) Guidelines for Smoking Cessation and Performance Coaching during Implementation Phase of the Study
Data collection from Patients: demographics, health status, smoking history, quitting behavior, perceptions of lung cancer risk and worry, impact of screening on tobacco use behavior, and exposure to the intervention. (baseline, \<14 days, 3 months, and 6 months)
Group II: Usual CareActive Control1 Intervention
No training or performance coaching calls on personnel, just usual clinic practice.
Data collection from Patients: demographics, health status, smoking history, quitting behavior, perceptions of lung cancer risk and worry, impact of screening on tobacco use behavior, and exposure to the intervention. (baseline, \<14 days, 3 months, and 6 months)
Smoking Cessation is already approved in United States, United States, United States, European Union, European Union, European Union for the following indications:
πΊπΈ Approved in United States as Nicotine Replacement Therapy for:
- Smoking cessation
πΊπΈ Approved in United States as Bupropion for:
- Smoking cessation
πΊπΈ Approved in United States as Varenicline for:
- Smoking cessation
πͺπΊ Approved in European Union as Nicotine Replacement Therapy for:
- Smoking cessation
πͺπΊ Approved in European Union as Bupropion for:
- Smoking cessation
πͺπΊ Approved in European Union as Varenicline for:
- Smoking cessation
Find a Clinic Near You
Research Locations NearbySelect from list below to view details:
University Medical Center of Southern NevadaLas Vegas, NV
Sanford South University Medical CenterFargo, ND
Aurora Saint Luke's Medical CenterMilwaukee, WI
Mercy Hospital WashingtonWashington, MO
More Trial Locations
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Who Is Running the Clinical Trial?
Wake Forest University Health SciencesLead Sponsor
National Cancer Institute (NCI)Collaborator