Smoking Cessation
Conditions
Keywords
lung cancer prevention
Brief summary
The purpose of this study is to develop and test a self-help smoking cessation treatment for patients receiving a lung cancer screening computed tomography (CT) scan.
Detailed description
Conduct Formative Research (Months 1 - 4): Identification of emergent themes and responses to existing booklets. Adapt and Refine Booklets (Months 5 - 8): Advanced drafts of booklets. Final Reactions to Draft Booklets (Months 9 - 12): Series of smoking cessation booklets for spiral computed tomography (CT) patients.
Interventions
BEHAVIORALSelf-Help (SHI)
The newly revised Stop Smoking for Good booklets.
BEHAVIORALUsual Care (UC)
The existing Clearing the Air smoking-cessation manual published by the National Cancer Institute (NCI).
Sponsors
James and Esther King Biomedical Research Program
H. Lee Moffitt Cancer Center and Research Institute
Study design
Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Study 1 * Participants for Study I will be drawn from a list of patients who have received a CT scan at the Moffitt Cancer Center * Smoked at least one cigarette per week prior to undergoing the CT scan * Able to speak and read English Study 2 * Smoked at least one cigarette over the past week * Able to read English
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Study 1 - Completion of Formative Evaluation | Up to 12 months | Complete formative research to adapt and refine the existing Stop Smoking for Good booklets. |
| Study 2 - Rate of Seven-Day Abstinence | Seven-day abstinence will be assessed at each follow-up, allowing for calculation of point-prevalence abstinence rates. For this pilot, we will not bioverify self-reported abstinence. | Up to 9 months |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Rate of Intervention Demand | Up to 9 months | Demand will be estimated by noting accrual rates into the study. |
| Degree of Practicality | Up to 9 months | Practicality encompasses the degree to which investigators are able to carry out all the piloted elements of the planned randomized control trial (RCT) successfully and efficiently (i.e., recruitment, screening, randomization, and follow-up). |
Countries
United States
Outcome results
None listed