Investigating the long-term impact of nicotine replacement products on tobacco smoking cessation for low-socioeconomic status smokers
Not Applicable
Recruiting
- Conditions
- Public Health - Health service researchMental Health - AddictionTobacco smoking
- Registration Number
- ACTRN12622001147774
- Lead Sponsor
- niversity of New South Wales
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 160
Inclusion Criteria
Participants can be included if they meet the primary outcome of six-month continuous abstinence in ACTRN12621000076875 (defined as self-report of having smoked less than or equal to 5 cigarettes in that time and carbon monoxide level of less than or equal to 5ppm using biochemical breath test verification) and provide informed consent.
Exclusion Criteria
There are no exclusion criteria.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Carbon monoxide (CO) verified 18-month continuous abstinence at 19-month follow-up. Continuous 18-month abstinence will be defined as having remained quit for 18-months (having smoked no more than five cigarettes in that time), and a carbon monoxide level of less-than-or-equal-to 5 parts per million. Depending on the participants indicated preference, the CO breath test will be self-administered using an using a hand-held iCO™ Smokerlyzer® (using provided instructions), or administered by a trained researcher using a hand-held iCO™ Micro+™ Smokerlyzer® with a disposable, one-use mouthpiece. [The follow-up interview will occur 19-months after the participant's baseline interview completion date for ACTRN12621000076875.]
- Secondary Outcome Measures
Name Time Method