Smoking Cessation Clinical Trial
Official title:
Capitalizing on a Teachable Moment to Promote Smoking Cessation
Verified date | August 2020 |
Source | H. Lee Moffitt Cancer Center and Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 35 |
Est. completion date | June 21, 2019 |
Est. primary completion date | June 21, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
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 |
Country | Name | City | State |
---|---|---|---|
United States | H Lee Moffitt Cancer Center | Tampa | Florida |
Lead Sponsor | Collaborator |
---|---|
H. Lee Moffitt Cancer Center and Research Institute | James and Esther King Biomedical Research Program |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Study 1 - Completion of Formative Evaluation | Complete formative research to adapt and refine the existing Stop Smoking for Good booklets. | Up to 12 months | |
Primary | Study 2 - Rate of Seven-Day Abstinence | Up to 9 months | 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. | |
Secondary | Rate of Intervention Demand | Demand will be estimated by noting accrual rates into the study. | Up to 9 months | |
Secondary | Degree of Practicality | 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). | Up to 9 months |
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