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STOP Study: Effectiveness of Zyban in a Clinical Population

The STOP Study: Real World Effectiveness of Zyban Treatment in a Clinical Population

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01015170
Enrollment
454
Registered
2009-11-18
Start date
2009-10-31
Completion date
2015-10-31
Last updated
2017-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cigarette Smoking, Nicotine Addiction, Smoking Cessation

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

Ontario Ministry of Health and Long Term Care
CollaboratorOTHER_GOV
Centre for Addiction and Mental Health
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frameDescription
7-day Point Prevalence of Smoking AbstinenceEnd 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

MeasureTime frameDescription
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 Abstinence6 months after Zyban start dateNumber 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

ArmCount
Buproprion & Behavioural Support
8 weeks of buproprion-SR + brief counselling for smoking cessation
454
Total454

Baseline characteristics

CharacteristicBuproprion & Behavioural Support
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
39 Participants
Age, Categorical
Between 18 and 65 years
415 Participants
Age, Continuous47.5 years
STANDARD_DEVIATION 13.2
Age first smoked14.1 years
STANDARD_DEVIATION 3.7
Age smoked daily16.4 years
STANDARD_DEVIATION 4.3
Cigarettes per day (cpd)20.5 # cigarettes smoked per day
STANDARD_DEVIATION 9
Confidence in quitting smoking7.6 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 smoking9.2 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 typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 454
serious
Total, serious adverse events
8 / 454

Outcome results

Primary

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

ArmMeasureGroupValue (NUMBER)
Nicotine Replacement & Behavioural Support7-day Point Prevalence of Smoking AbstinenceStill smoking109 participants
Nicotine Replacement & Behavioural Support7-day Point Prevalence of Smoking AbstinenceQuit smoking106 participants
Secondary

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

ArmMeasureCategoryValue (COUNT_OF_PARTICIPANTS)
Nicotine Replacement & Behavioural Support7-day Point Prevalence of Smoking AbstinenceSmoked in past 7 days320 Participants
Nicotine Replacement & Behavioural Support7-day Point Prevalence of Smoking AbstinenceDid not smoke in past 7 days128 Participants
Secondary

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.

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026