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Poor recruitment
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A placebo-controlled trial to determine whether recent ex-smokers with COPD who successfully stop smoking after taking varenicline are less likely to relapse back to smoking if they continue using varenicline for a further 12 weeks
Smoking remains the leading cause of Chronic Obstructive Pulmonary Disease (COPD), a leading cause of death and disability in New Zealand. COPD particularly affects indigenous Māori and Pacific people, given their higher rates of smoking. COPD patients tend to have a higher level of nicotine dependence and, as a result, often find quitting harder and are more likely to relapse back to smoking. A clinical trial (N=262) is planned in Auckland, New Zealand to determine whether extended varenicline treatment combined with behavioural support can prevent relapse back to smoking in recent ex-smokers with COPD. Smoking cessation and relapse prevention are the most cost-effective interventions available for COPD patients that smoke, irrespective of their disease stage. The trial has the potential to significantly improve the outcomes of this common and chronic health condition in New Zealand.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Varenicline plus behavioural support | Active Comparator | 12 weeks extended treatment with varenicline, plus relapse prevention-orientated behavioural support |
|
| Placebo plus behavioural support | Placebo Comparator | 12 weeks extended treatment with placebo, plus relapse prevention-orientated behavioural support |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Varenicline | Drug | Two 0.5mg tablets taken twice daily |
|
| Measure | Description | Time Frame |
|---|---|---|
| Continuous abstinence | Continuous (lapse-free) abstinence biochemically validated using a carbon monoxide reading of <10 ppm. | 12 weeks post-randomisation |
| Measure | Description | Time Frame |
|---|---|---|
| Continuous abstinence | Biochemically validated continuous (lapse-free) abstinence | 24 weeks post-randomisation |
| 7-day point prevalence abstinence | Biochemically validated 7-day point prevalence abstinence, defined as no smoking in the last seven days, not even a puff. |
| Measure | Description | Time Frame |
|---|---|---|
| Medication adherence (Script redeemed) | Question asked about whether they redeemed their allocated script | 12 weeks post-randomisation |
| Question about medication compliance (pill count). | Ask about how many of their allocated pills they took |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Natalie Walker, PhD | University of Auckland, New Zealand | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| National Institute for Health Innovation, University of Auckland | Auckland | New Zealand |
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| ID | Term |
|---|---|
| D029424 | Pulmonary Disease, Chronic Obstructive |
| D016540 | Smoking Cessation |
| ID | Term |
|---|---|
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002908 | Chronic Disease |
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| ID | Term |
|---|---|
| D000068580 | Varenicline |
| ID | Term |
|---|---|
| D001552 | Benzazepines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
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| Behavioural support | Behavioral | Consisting of the study-specific doctor delivering relapse prevention orientated behavioural support at the time of consultation, plus six 10-15 minute calls over the 12 weeks delivered by a research assistant. |
|
| Placebo | Drug | Two 0.5mg tablets taken twice daily |
|
| 12 weeks post-randomisation |
| 7-day point prevalence abstinence | Biochemically validated 7-day point prevalence abstinence, defined as no smoking in the last seven days, not even a puff. | 24 weeks post-randomisation |
| Time to lapse | Time to first lapse, defined as time to first cigarette smoked (even a puff) | 12 weeks post-randomisation |
| Time to lapse | Time to first lapse, defined as time to first cigarette smoked (even a puff) | 24 weeks post-randomisation |
| Time to relapse | Time to first relapse, defined as smoking ≥five cigarettes a day for three consecutive days. | 12 weeks post-randomisation |
| Time to relapse | Time to first relapse, defined as smoking ≥five cigarettes a day for three consecutive days. | 24 weeks post-randomisation |
| Cigarettes per day | Cigarettes smoked per day, if returned to smoking | 12 weeks post-randomisation |
| Cigarettes per day | Cigarettes smoked per day, if returned to smoking | 24 weeks post-randomisation |
| COPD exacerbations requiring hospitalisation | The number of COPD exacerbations in the past 12 weeks, defined as a worsening of COPD respiratory symptoms that resulted in a course of antibiotics and/or oral steroids; or an unscheduled visit to GP, urgent care, Emergency Department or as an inpatient. Data will be validated against medical records using data linkage. | 12 weeks post-randomisation |
| COPD exacerbations requiring hospitalisation | The number of COPD exacerbations in the past 12 weeks, defined as a worsening of COPD respiratory symptoms that resulted in a course of antibiotics and/or oral steroids; or an unscheduled visit to GP, urgent care, Emergency Department or as an inpatient. Data will be validated against medical records using data linkage. | 24 weeks post-randomisation |
| Urge to smoke/cravings | The physical signs and symptoms associated with withdrawal will be measured using the Mood and Physical Symptoms Scale (MPSS). | 12 weeks post-randomisation |
| Urge to smoke/cravings | The physical signs and symptoms associated with withdrawal will be measured using the Mood and Physical Symptoms Scale (MPSS). | 24 weeks post-randomisation |
| Cigarette dependence | Cigarette dependence, as measured by the Fagerström Test of Cigarette Dependence | 12 weeks post-randomisation |
| Cigarette dependence | Cigarette dependence, as measured by the Fagerström Test of Cigarette Dependence | 24 weeks post-randomisation |
| Health-related quality of life | Measured using the EQ-5D | 12 weeks post-randomisation |
| Health-related quality of life | Measured using the EQ-5D | 24 weeks post-randomisation |
| Serious adverse events | 12 weeks post-randomisation |
| Serious adverse events | 24 weeks post-randomisation |
| 12 weeks post-randomisation |
| Question about use of other cessation products | Questions will be asked about whether other cessation products were used and if so, what type. E-cigarettes will be considered a possible cessation product. | 12 weeks post-randomisation |
| Questions asked about the use of other cessation products | Questions will be asked about whether other cessation products were used and if so, what type. E-cigarettes will be considered a possible cessation product. | 24 weeks post-randomisation |
| D020969 |
| Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D015438 | Health Behavior |
| D001519 | Behavior |
| D011810 | Quinoxalines |