SUCCESS STUDY; Smoking reduction by a smoking cessation strategy in the national cervical cancer screening program
- Conditions
- tabaksverslavingcervical cancer screeningsmoking cessation10001474
- Registration Number
- NL-OMON44561
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Withdrawn
- Sex
- Not specified
- Target Recruitment
- 660
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- Participating in the national cervical cancer screening program, i.e. undergoing a cervical smear at a general practice included in the study, upon invitation from the national cervical screening program organization. This includes those women undergoing a smear after they are found to be HPV-positive after a self-test provided by the national cervical cancer screening organization.
- Able to communicate in Dutch.
- Given informed consent for participation in a study about lifestyle. ;In order to be identified as a smoker, a subject must meet one of the following criteria:
- Daily or non-daily smokers who participate in cervical cancer screening, identified at baseline via the baseline questionnaire T1 or upon inquiry from the practice assistant about the screening participants* smoking status
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- Undergoing a cervical smear at the general practice NOT upon an invitation from the national cervical screening program organization.
- Not able to communicate in Dutch.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary outcome includes performing a serious quit attempt (any attempt<br /><br>lasting >24 hours). The percentage of smoking participants (at baseline) who<br /><br>performed a serious quit attempts during the follow-up period will be measured.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary outcomes include the total number of quit attempts per participants.<br /><br>The point prevalence abstinence will be measured (defined as not smoking during<br /><br>the last 7 prior to filling in the questionnaire at 6 months follow-up). The<br /><br>total number of smoked cigarettes per day (reduction in number of cigarettes)<br /><br>and the transition in stage of change, e.g. change of motivation to quit<br /><br>smoking, will be measured.</p><br>
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