Motivating a Spectrum of Cancer Patients to Quit Smoking: Intervention Development and Feasibility
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Cancer
- Sponsor
- H. Lee Moffitt Cancer Center and Research Institute
- Enrollment
- 53
- Locations
- 1
- Primary Endpoint
- Number of Participants Who Read the Booklet - Demand - 1 Week Post Treatment
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
This study will assess feasibility and acceptability of an intervention designed to increase smoking cessation motivation among patients with a cancer not widely known to be smoking related.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Smoking at least 1 cigarette in previous 30 days
- •Diagnosis of breast, colorectal, gynecological, skin melanoma, or bladder cancer within the last 6 months
- •Able to read/write English
- •Able to give informed consent
- •Not currently enrolled in a smoking cessation program
Exclusion Criteria
- •Having distant metastases
- •Male patients with breast cancer
Outcomes
Primary Outcomes
Number of Participants Who Read the Booklet - Demand - 1 Week Post Treatment
Time Frame: 1-week post-treatment
Number of study participants who read the booklet
Number of Participants Who Read the Booklet - Demand - 1 Month Post Treatment
Time Frame: 1-month post-treatment
Number of study participants who read the booklet
Number of Participants That Complete 1-week Follow-up Assessments - Feasibility
Time Frame: 1-week post-treatment
Number of participants who complete 1-week follow-up assessments
Number of Participants That Complete 1 Month Follow-up Assessments - Feasibility
Time Frame: 1-month post-treatment
Number of participants who complete 1-month follow-up assessments
Number of Participants Who Consent to Participate in the Study- Feasibility
Time Frame: Baseline
Number of participants who consent to participate in the study
Acceptability
Time Frame: 1-month post-treatment
Treatment satisfaction measured with 8 items adapted from the Client Satisfaction Questionnaire, values between 8 and 32, with higher scores mean a better outcome.
Secondary Outcomes
- Participants Change in Motivation - Action Stage(Baseline, at 1 week and 1 month post treatment)
- Number of Participants Reporting 7-day Point Prevalence Abstinence(1-week post-treatment)
- Number of Participants Reporting 30-day Point Prevalence Abstinence(1-month post-treatment)
- Motivation to Quit Smoking Assessed With the Contemplation Ladder(Baseline, 1-week post-treatment, 1-month post-treatment)
- Motivation to Quit Smoking Assessed With the Short Form of the Smoking Abstinence-related Motivational Engagement (ARME).(Baseline, 1-week post-treatment, 1-month post-treatment)
- Motivation to Quit Smoking Assessed With the Number of Visits to the Study Website(1-month post-treatment)
- Motivation to Quit Smoking Assessed by Contact With the Tobacco Treatment Specialist - 1 Month(At 1 Month Post Treatment)
- Participants That Had a Quit Attempt - 1 Week(At 1 Week Post Treatment)
- Participants That Had a Quit Attempt - 1 Month(At 1 Month Post Treatment)
- Motivation to Quit Smoking Assessed With the Number of Quit Attempts - 1 Month(At 1 Month Post Treatment)
- Motivation to Quit Smoking Assessed by Contact With the Tobacco Treatment Specialist - 1 Week(At 1 Week Post Treatment)