Cigarette Smoking, Nicotine Addiction, Smoking Cessation
Conditions
Keywords
smoking cessation, nicotine addiction, Zyban, bupropion hydrochloride
Brief summary
Despite the significant health, social and economic costs of cigarette smoking, 17% of Ontarians still currently smoke. Use of smoking cessation pharmacotherapy such as Zyban (bupropion HCl) has been shown to double quit rates but such medications are under-utilized by smokers attempting to quit. It has been suggested that the high price of pharmacotherapy may act as a barrier to accessing such treatment.The main objective of this study is to evaluate the methods and effectiveness of providing smokers who want to quit with 8 weeks of free Zyban in combination with smoking cessation counselling through family health teams and community health centres across the province. Hypothesis: Ontario smokers who receive 8-weeks of free bupropion in combination with brief counselling will have higher smoking cessation rates than the standard population cessation rates.
Detailed description
Nicotine dependence, like other addictive disorders, can be characterized as a chronic, relapsing disease (Leshner, 1997). Although there is significant morbidity and mortality associated with this disorder, the majority of smokers are not treated adequately to the widely accepted goal of complete long-term abstinence from smoking. This may be due to the under-utilization of accepted pharmacotherapies for the treatment of tobacco dependence. Bupropion (Zyban) Bupropion is the first line of non-nicotine-based pharmacotherapy for smoking cessation. Several large-scale clinical trials have shown bupropion to be an efficacious smoking cessation aid (Hurt et al., 1997; Jorenby et al., 1999; Ahluwalia et al., 2002). In one such study, a 44% abstinence rate was reported for seven weeks of treatment with bupropion at 300 mg/day, compared to 19% for placebo (Hurt et al, 1997). A recent meta-analysis has reported that bupropion monotherapy approximately doubles the rate of smoking cessation (OR 1.94) (Hughes et al, 2007). Despite its efficacy, bupropion's mechanism of action is unclear. Attenuation of abstinence-associated increase in craving and withdrawal symptoms has been suggested as possible mechanisms of bupropion's effect on smoking behaviour in a few randomized clinical trials (Jorneby et al., 1999; Shiffman et al., 2000; Lerman et al., 2002; Durcan et al, 2002). However, these effects are not universally demonstrated (Hurt et al., 1997; Shiffman et al., 2000). Other possible bio-behavioral mechanisms have remained largely unexplored. Using positron emission tomography (PET) it has been shown that in contrast to untreated smokers, when bupropion-treated smokers were exposed to cigarette-related cues there was less metabolic activation in their anterior cingulate cortex, a region of the brain previously shown to be activated by cigarette cues (Brody et al., 2004;Brody et al., 2002). STOP Study Background and Rationale Treatment with pharmacotherapy such as nicotine replacement therapy (NRT) or Zyban is a safe and effective smoking cessation strategy that can double the chance of quitting successfully over the long-term (Cornuz, 2007). However, research has shown that most smokers who are interested in quitting do not use pharmacotherapy to aid in their quit attempt. Misconceptions about the harmful effects of nicotine are a strong barrier to the use of pharmacotherapy. The cost of pharmacotherapy may also be a significant contributor to the under-utilization of smoking cessation aids such as NRT and Zyban. Karnath (2001) suggested that the high cost of successful pharmacotherapy treatment for smoking cessation may be a barrier for some individuals. Moreover, Cokkinides et al (2005) reported that smokers with private insurance were more likely to use smoking cessation pharmacotherapies than smokers without insurance. The addition of free NRT to a group behavioural cessation program substantiated these claims by showing an increase in quit rates from 38% to 65% (Alberg et al, 2004). These studies suggest that economic barriers may prevent smokers from using pharmacotherapy in their attempts to quit smoking. The study proposed herein will introduce free bupropion as another treatment option for smoking cessation for Ontario smokers. Community Health Centres and Aboriginal Health Access Centres are interdisciplinary health models that are able to help individuals who would otherwise be prevented from accessing health services due to social and geographic barriers. As they aim to eliminate these other barriers and consequently control for them, they are an ideal health model for determining whether eliminating the economic barriers of smoking cessation improves smoking cessation rates. Family Health Teams are more recent health models that provide integrated and interdisciplinary primary health care. Since they are able to treat large and diverse populations, they are an ideal health model for accessing Ontario smokers. Objectives 1\. To evaluate the effectiveness of 8-weeks of free bupropion in combination with brief counselling through family health teams, community health centres and aboriginal health access centres in Ontario for smoking cessation.
Interventions
150mg BID for up to 8 weeks + counseling
Sponsors
Study design
Eligibility
Inclusion criteria
* Ontario resident * 18 years of age or older * Current daily cigarette smoker who smokes 10 or more cigarettes per day and has smoked \> 100 cigarettes in their lifetime * Want to quit smoking cigarettes within 30 days of assessment * Willingness and capacity to give written informed consent and to comply with study protocol
Exclusion criteria
* Enrollment in any of the STOP Study NRT models in the past 6 months * Currently receiving Wellbutrin SR or any medication containing bupropion hydrochloride * Current seizure disorder or history of seizures * Current or prior diagnosis of bulimia or anorexia nervosa * Current diagnosis of bipolar disorder * History of head trauma * Allergy or sensitivity to Zyban, Wellbutrin or bupropion * Undergoing abrupt withdrawal from alcohol, benzodiazepines or other sedatives * Currently taking monoamine oxidase (MAO) inhibitors, or thioridazine * Pregnant or breastfeeding or at risk of becoming pregnant * Central nervous system (CNS) tumor * Severe hepatic impairment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 7-day Point Prevalence of Smoking Abstinence | End of Treatment (8 weeks after Zyban start date) | Number of participants who report Not Smoking (not even a puff) in past 7 days when asked at week 8 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Serious Quit Attempt (at Least 24 Hours of Abstinence) | End of Treatment (8 weeks after Zyban start date) | Number of participants who report a serious quit attempt at End of treatment |
| 7-day Point Prevalence of Smoking Abstinence | 6 months after Zyban start date | Number of participants who report Not Smoking (not even a puff) in past 7 days when asked 6 months after Zyban start date |
Countries
Canada
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Buproprion & Behavioural Support 8 weeks of buproprion-SR + brief counselling for smoking cessation | 454 |
| Total | 454 |
Baseline characteristics
| Characteristic | Buproprion & Behavioural Support |
|---|---|
| Age, Categorical <=18 years | 0 Participants |
| Age, Categorical >=65 years | 39 Participants |
| Age, Categorical Between 18 and 65 years | 415 Participants |
| Age, Continuous | 47.5 years STANDARD_DEVIATION 13.2 |
| Age first smoked | 14.1 years STANDARD_DEVIATION 3.7 |
| Age smoked daily | 16.4 years STANDARD_DEVIATION 4.3 |
| Cigarettes per day (cpd) | 20.5 # cigarettes smoked per day STANDARD_DEVIATION 9 |
| Confidence in quitting smoking | 7.6 units on a scale STANDARD_DEVIATION 2 |
| Education level attained missing | 9 participants |
| Education level attained Post secondary | 207 participants |
| Education level attained up to highschool | 238 participants |
| Employment Employed | 221 participants |
| Employment missing | 4 participants |
| Employment Not employed | 229 participants |
| Ever had a psychiatric diagnosis No | 309 participants |
| Ever had a psychiatric diagnosis Yes | 145 participants |
| Importance of quitting smoking | 9.2 units on a scale STANDARD_DEVIATION 1.3 |
| Income category missing | 87 participants |
| Income category more than $40,000 | 106 participants |
| Income category up to $40,000 | 261 participants |
| # quit attempts in the past 0 - 2 quit attempts | 181 participants |
| # quit attempts in the past 3 or more quit attempts | 225 participants |
| # quit attempts in the past missing | 48 participants |
| Sex: Female, Male Female | 243 Participants |
| Sex: Female, Male Male | 211 Participants |
| Time to first morning cigarette 15 minutes or less | 306 participants |
| Time to first morning cigarette missing | 4 participants |
| Time to first morning cigarette more than 15 minutes | 144 participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | — / — |
| other Total, other adverse events | 0 / 454 |
| serious Total, serious adverse events | 8 / 454 |
Outcome results
7-day Point Prevalence of Smoking Abstinence
Number of participants who report Not Smoking (not even a puff) in past 7 days when asked at week 8
Time frame: End of Treatment (8 weeks after Zyban start date)
Population: Participants who completed survey 8 weeks after Zyban start date
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Nicotine Replacement & Behavioural Support | 7-day Point Prevalence of Smoking Abstinence | Still smoking | 109 participants |
| Nicotine Replacement & Behavioural Support | 7-day Point Prevalence of Smoking Abstinence | Quit smoking | 106 participants |
7-day Point Prevalence of Smoking Abstinence
Number of participants who report Not Smoking (not even a puff) in past 7 days when asked 6 months after Zyban start date
Time frame: 6 months after Zyban start date
Population: Number of participants who completed 6 month post treatment survey
| Arm | Measure | Category | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Nicotine Replacement & Behavioural Support | 7-day Point Prevalence of Smoking Abstinence | Smoked in past 7 days | 320 Participants |
| Nicotine Replacement & Behavioural Support | 7-day Point Prevalence of Smoking Abstinence | Did not smoke in past 7 days | 128 Participants |
Serious Quit Attempt (at Least 24 Hours of Abstinence)
Number of participants who report a serious quit attempt at End of treatment
Time frame: End of Treatment (8 weeks after Zyban start date)
Population: This secondary outcome was not collected at 8 week followup.