Abstract
BackgroundSmoking rates are higher in New Zealand (NZ) adults with mental illnesses and alcohol and other drug (AOD) addictions, compared to the overall population. Quit attempts using “gold standard” smoking cessation treatments often fail in people with these conditions, so more flexible treatment regimens that adapt to a person’s responsiveness to treatment are worth investigating. The STATUS trial aims to evaluate the effectiveness and safety of combining varenicline with nicotine e-cigarettes for smoking cessation among varenicline non-responders in treatment for mental health illnesses and/or AOD addictions.MethodsThis is a pragmatic two-arm, open-label, randomised trial. Participants will be daily smokers using mental health and/or addiction services in Auckland, aged ≥18 years, motivated to quit smoking, and eligible to access varenicline through the NZ special authority process. After 2 weeks of using varenicline plus behavioural support, participants who have not reduced their daily smoking by ≥50% will be randomised (1:1) to either 10 weeks of continued varenicline use or 10 weeks of varenicline plus an 18 mg/mL nicotine e-cigarette. All participants will receive weekly withdrawal-orientated behavioural support calls for 6 weeks post-randomisation. The primary outcome is self-reported biochemically-verified (exhaled carbon monoxide) continuous abstinence at 24 weeks post-randomisation. Secondary outcomes, measured at six, 12 and 24 weeks post-randomisation include: self-reported continuous abstinence, 7-day point prevalence abstinence, smoking reduction, time to relapse, cross-over, use of other smoking cessation support, serious adverse events, treatment adherence, compliance, acceptability, dual use, continuation of treatment use, mental illness symptoms and AOD use, health-related quality of life, and cost-analysis. A sample size of 338 will confer 80% power (p = 0.05) to detect a 15% absolute difference between the varenicline alone and varenicline plus e-cigarette groups.DiscussionPeople with mental illness and/or AOD addictions are just as motivated as others to quit smoking, but are less likely to succeed. Adapting smoking cessation medication after a lack of responsiveness in the first 2 weeks of initial treatment in this priority population by adding a nicotine e-cigarette may be one way to increase long-term quit rates.Trial RegistrationAustralian NZ Clinical Trial Registry: ACTRN12616001355460 (29 September 2016).
Highlights
Smoking rates are higher in New Zealand (NZ) adults with mental illnesses and alcohol and other drug (AOD) addictions, compared to the overall population
Smoking prevalence in the New Zealand (NZ) adult population has declined from 25% in 1996 to 16% in 2017 [1], but among people with mental illnesses and/or alcohol and other drug (AOD) addictions the prevalence of smoking has remained far higher: among people with a self-reported mental illness there was only a slight decrease from 33% in 1996, to 29% in 2012 [2]
The rationale for this design is based on the finding that smokers who reduce their cigarette consumption by at least 50% during the first 2 weeks after starting on either varenicline or nicotine replacement treatment (NRT) are 2 to 3 times more likely to quit for the long-term than smokers who do not experience this positive medication response (‘non-responders’) [23, 32,33,34]
Summary
Design The following trial protocol (version 4.0, 1 November 2017) adheres to the SPIRIT guidelines (Additional file 1). The research assistant will phone participants two weeks after they have started their treatment, to assess their response to varenicline Those who are varenicline responders (i.e. they have quit smoking or reduced the number of cigarettes smoked per day by > 50%) will be advised to continue their use of varenicline for another 10 weeks and to contact Quitline and/or a health professional (general practitioner or head clinician) for on-going smoking cessation behavioural support.
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