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Trial registered on ANZCTR
Registration number
ACTRN12612000914864
Ethics application status
Approved
Date submitted
27/08/2012
Date registered
28/08/2012
Date last updated
28/05/2013
Type of registration
Prospectively registered
Titles & IDs
Public title
Nicotine Reduction Pilot Study
To determine if a price differential based on nicotine content reduces cigarette consumption in smokers who are unmotivated to quit.
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Scientific title
Nicotine Reduction Study using very low nicotine content cigarettes (VLNC) in smokers who are unmotivated to quit
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Secondary ID [1]
281099
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Nil
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Universal Trial Number (UTN)
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Trial acronym
ENRIQ- Evaluation of Nicotine Reduction in Queenstown
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Smoking Cessation
287257
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Condition category
Condition code
Public Health
287584
287584
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0
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Epidemiology
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Mental Health
287592
287592
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0
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Addiction
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention arm: Very low nicotine content (VLNC) cigarettes will be given to the intervention group for eight weeks. The number of VLNC provided will be based on the number of nicotine containing cigarettes they usually smoke at baseline.
Each participant will be able to smoke as many of the VLNC as they wish during the eight weeks intervention.
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Intervention code [1]
285552
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Treatment: Other
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Intervention code [2]
285560
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Lifestyle
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Comparator / control treatment
Active arm: Will be requested to purchase their usual brand of cigarettes over the eight weeks. They will be asked to smoke as many of their usual brand of cigarettes as they wish during the eight weeks.
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Control group
Active
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Outcomes
Primary outcome [1]
287840
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The change from baseline in the mean number of regular cigarettes smoked in the past week, measured at 12 weeks. Each participant will be requested daily via text message to submit the number of cigarettes they smoked the day before.
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Assessment method [1]
287840
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Timepoint [1]
287840
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12 weeks
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Secondary outcome [1]
298914
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Mean number of regular cigarettes smoked each week calculated by adding daily text messages results of the number of cigarettes smoked or where no text is received via telephone call request for the information (self reported).
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Assessment method [1]
298914
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Timepoint [1]
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1,2,3,4,5,6,9 and 12 weeks
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Secondary outcome [2]
298915
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Salivary cotinine measurement
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Assessment method [2]
298915
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Timepoint [2]
298915
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1,2,3,4,5,6,9 and 12 weeks
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Secondary outcome [3]
298916
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Nicotine dependence, including time to first cigarette using the Fagerstrom Test for Nicotine dependence questionnaire.
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Assessment method [3]
298916
0
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Timepoint [3]
298916
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6 and 12 weeks
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Secondary outcome [4]
298917
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Smoking satisfaction and craving reduction using the modified Cigarette Evaluation Questionnaire (mCEQ).
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Assessment method [4]
298917
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Timepoint [4]
298917
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6 and 12 weeks
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Secondary outcome [5]
298918
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The behavioural components of smoking addiction using the Glover Nilsson Smoking Behavioural Questionnaire.
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Assessment method [5]
298918
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Timepoint [5]
298918
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6 and 12 weeks
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Secondary outcome [6]
298919
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Autonomy over smoking using the AUTOS Questionnaire
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Assessment method [6]
298919
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Timepoint [6]
298919
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6 and 12 weeks
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Secondary outcome [7]
298920
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Changes in the physical signs and symptoms of nicotine withdrawal and craving
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Assessment method [7]
298920
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Timepoint [7]
298920
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6 and 12 weeks
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Secondary outcome [8]
298921
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Self-rated chances of quitting using the Self- efficacy questionnaire (1-5 scale).
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Assessment method [8]
298921
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Timepoint [8]
298921
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6 and 12 weeks
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Secondary outcome [9]
298922
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Quitting behaviour: 7-day point prevalence continuous abstinence rates, defined as the proportion of particpants who consumed no "regular" cigarettes (not even a single puff) in the previous seven days (self reported). Use of nicotine and non-nicotine methods of quitting support via questionnaire.
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Assessment method [9]
298922
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Timepoint [9]
298922
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6 and 12 weeks
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Secondary outcome [10]
298923
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Views on a nicotine reduction strategy collected via questionnaire covering concerns, likes, dislikes etc.
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Assessment method [10]
298923
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Timepoint [10]
298923
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12 weeks
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Eligibility
Key inclusion criteria
they do not wish to quit smoking in the next three months
they are at least 18 years of age
they are daily smokers
their time to first cigarette is within 30 minutes of waking
they are able to provide written consent
they have a mobile phone they can use daily
they have a mobile phone that is capable of receiving and sending text messages
they intend to reside in the Otago/Southland region for the next six months
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Pregnant women
Women who are breastfeeding
Current users of NRT products (including electronic cigarettes with nicotine)
Currently enrolled in a quit smoking programme (such as Quitline)
Current users of non-nicotine based cessation therapies (e.g. buproprion, clonidine, nortriptyline or varenicline)
Only use non-cigarette tobacco products (e.g. pipes, cigars).
One person per household can be recruited into the study.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Participants will be centrally randomised by computer using allocation concealment
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Participants will be randomised using dynamic allocation/stratified minimisation by sex, ethnicity, and level of nicotine dependence (as determined by the Fagerstrom Test for Nicotine Dependence)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/12/2012
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Actual
6/11/2012
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Date of last participant enrolment
Anticipated
14/12/2012
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Actual
15/12/2012
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
60
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
4511
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New Zealand
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State/province [1]
4511
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Otago region (South Island)
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Funding & Sponsors
Funding source category [1]
285884
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Government body
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Name [1]
285884
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Health Reseach Council (HRC NZ)
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Address [1]
285884
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PO Box 5541, Wellesley Street, Auckland 1141
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Country [1]
285884
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New Zealand
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Primary sponsor type
University
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Name
National Institute For Health Innovation (NIHI)
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Address
University of Auckland
Private Bag 92019
Auckland Mail Centre
Auckland 1142
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Country
New Zealand
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Secondary sponsor category [1]
284709
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None
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Name [1]
284709
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Address [1]
284709
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Country [1]
284709
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Other collaborator category [1]
277039
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University
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Name [1]
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Centre for Tobacco Control Research
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Address [1]
277039
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School of Population Health Research
University of Auckland
Private Bag 92019
Auckland Mail Centre
Auckland 1142
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Country [1]
277039
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New Zealand
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Other collaborator category [2]
277040
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Commercial sector/Industry
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Name [2]
277040
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ESR Ltd
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Address [2]
277040
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Hampstead Road
Sandringham
Auckland 1142
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Country [2]
277040
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New Zealand
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Other collaborator category [3]
277041
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Commercial sector/Industry
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Name [3]
277041
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Global Public Health Ltd
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Address [3]
277041
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Po Box 82
Glenorchy 9350
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Country [3]
277041
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New Zealand
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Other collaborator category [4]
277042
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Commercial sector/Industry
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Name [4]
277042
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Health New Zealand Ltd
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Address [4]
277042
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36 Winchester St, Lyttelton
Christchurch 8082
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Country [4]
277042
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New Zealand
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
287913
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Heath And Disabilty Ethics Committee, Northern B
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Ethics committee address [1]
287913
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Ministry of Health 1 The Terrace PO BOX 5013 Wellington 6011
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Ethics committee country [1]
287913
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New Zealand
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Date submitted for ethics approval [1]
287913
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01/10/2012
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Approval date [1]
287913
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01/11/2012
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Ethics approval number [1]
287913
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12/NTB/48
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Summary
Brief summary
In order to reach the government’s goal to have a smokefree New Zealand by 2025, radical changes need to be made at both the policy and practical level as the ‘business as usual’ approach to smoking cessation will not achieve the goal. A nicotine reduction strategy is one approach that may help reduce the level of nicotine dependence in smokers, resulting in a greater chance of quitting. However, insufficient data exist on what would happen if a nicotine reduction policy was implemented, or what form such a policy should take.
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Trial website
http://www.turanga.org.nz/ http://nihi.auckland.ac.nz/index.php
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
34625
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Dr Natalie Walker
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Address
34625
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University of Auckland
National Institute For Health Innovation
Private Bag 92019
Auckland 1142
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Country
34625
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New Zealand
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Phone
34625
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+64 9 923 9884
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Fax
34625
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Email
34625
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[email protected]
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Contact person for public queries
Name
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Dr Colin Howe
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Address
17872
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NIHI
University of Auckland
Private Bag 92019
Auckland Mail Centre
Auckland 1142
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Country
17872
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New Zealand
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Phone
17872
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+64 9 923 4765
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Fax
17872
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+64 9 373 1710
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Email
17872
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[email protected]
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Contact person for scientific queries
Name
8800
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Dr Natalie Walker
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Address
8800
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NIHI
University of Auckland
Private Bag 92019
Auckland Mail Centre
Auckland 1142
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Country
8800
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New Zealand
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Phone
8800
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+64 9 923 9884
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Fax
8800
0
+64 9 373 1710
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Email
8800
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Abrupt nicotine reduction as an endgame policy: a randomised trial.
2015
https://dx.doi.org/10.1136/tobaccocontrol-2014-051801
N.B. These documents automatically identified may not have been verified by the study sponsor.
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