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Trial registered on ANZCTR
Registration number
ACTRN12617000252314
Ethics application status
Approved
Date submitted
16/02/2017
Date registered
17/02/2017
Date last updated
20/07/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Evaluating a Computer-based Inhibitory Smoking Training (INST) program to assist individuals to quit or reduce smoking.
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Scientific title
A Randomised Controlled Trial examining the Efficacy of Training Response Inhibition to Smoking in Nicotine Dependent Individuals.
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Secondary ID [1]
291068
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nil
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Universal Trial Number (UTN)
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Trial acronym
Inhibitory Smoking Training (INST)
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Linked study record
N/A
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Health condition
Health condition(s) or problem(s) studied:
Smoking
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Addiction
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Nicotine dependence
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Condition category
Condition code
Mental Health
301545
301545
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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
The intervention is an online GoNoGo response inhibition training task as developed by Lawrence et al. (2015). The task used in this study has been modified to incorporate images of smoking. The intervention will consist of smoking-related pictures, non-smoking behaviour-related pictures, and neutral pictures. The neutral pictures are incorporated to prevent participants from easily identifying the associative rules of the task such that learning will occur through automatic processes as opposed to explicit control. Smoking-related pictures will always be paired with no-go signals, non-smoking pictures will always be paired with go signals, and neutral pictures will be paired equally with go and no-go signals. The training will consist of 6 blocks of 36 trials in each block. There are 14 sessions altogether which occur once a day for two weeks. Participants must quickly indicate whether the picture is located to the left or the right of the computer screen on their keyboard ('go' trials). On half of the trials, the frame around the picture will be bolded ('no go' cue) and the participants must not respond. Participants will be provided with feedback on their accuracy and mean go reaction time at the end of each block. Each training session will last for approximately 10 minutes. T
Reference: Lawrence, N. S., O’Sullivan, J., Parslow, D., Javaid, M., Adams, R. C., Chambers, C. D., … Verbruggen, F. (2015). Training response inhibition to food is associated with weight loss and reduced energy intake. Appetite, 95, 17–28. doi:10.1016/j.appet.2015.06.009
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Intervention code [1]
297056
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Behaviour
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Intervention code [2]
297057
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Lifestyle
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Comparator / control treatment
The active control is a general inhibition training task and is in the same format as the intervention, except only contains neutral pictures. The active control training is identical to that described in Lawrence et al. (2015).
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Control group
Active
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Outcomes
Primary outcome [1]
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Smoking cessation Yes/No
Measured by the Timeline Follow Back method (Sobell & Sobell, 1976)
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Assessment method [1]
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Timepoint [1]
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Post-intervention, 1-month follow-up, 3-month follow-up
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Primary outcome [2]
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Number of cigarettes smoked
Measured by the Timeline Follow Back method (Sobell & Sobell, 1976)
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Assessment method [2]
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Timepoint [2]
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Post-intervention, 1-month follow-up, 3-month follow-up
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Secondary outcome [1]
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Nicotine Craving
Smoking Craving Questionnaire (Johnson 2001)
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Assessment method [1]
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Timepoint [1]
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Post-intervention, 1-month follow-up, 3-month follow-up
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Secondary outcome [2]
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Self-efficacy
Visual analogue Scale "How confident do you feel right now that you can achieve your goal reducing/quitting smoking"
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Assessment method [2]
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Timepoint [2]
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Post-intervention, 1-month follow-up, 3-month follow-up
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Secondary outcome [3]
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Severity of nicotine dependence
Fagerstrom measure of Nicotine Dependence
Heatherton, Kozlowski, Frecker, Fagerstrom (1991)
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Assessment method [3]
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Timepoint [3]
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Post-intervention, 1-month follow-up, 3-month follow-up
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Secondary outcome [4]
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Impulsivity - behavioural and self-report
Barratt measure of impulsivity (BIS II) (self-report)
Stop Signal Task (behavioural)
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Assessment method [4]
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Timepoint [4]
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Post-intervention, 1-month follow-up, 3-month follow-up
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Secondary outcome [5]
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Positive valence towards smoking cues
Smoking specific Valence measure adapted from Lawrence et al 2015
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Assessment method [5]
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Timepoint [5]
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Post-intervention, 3-month follow-up
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Eligibility
Key inclusion criteria
Regular cigarette use- smokes 10 or more cigarettes per day on average for at least the past 12 months
DSM V Diagnosis of Tobacco Use Disorder
Reside in Melbourne Metropolitan Area (need to meet them face to face)
Completed at least year 9 at a mainstream school or equivalent
Regular access to a computer and internet on a daily basis for the next two week
Express an intention to reduce or quit smoking
Between the ages of 18 - 60
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Minimum age
18
Years
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Maximum age
60
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
High risk use of alcohol or drugs (other than nicotine)
No period of abstinence from nicotine (excluding e.g. hospital stays) longer than 2 weeks in the past 3 months
Reports of a brain injury or a loss of consciousness for more than 30 minutes
Currently using anti-craving medication such as Champix (varenicline) or Zyban (buproprion)
Use of psychotropic medications such as antidepressants, anxiolytics or antipsychotics
Primary nicotine use is via e-cigarettes
Individuals who use nicotine replacement therapy (e.g. Nicorette patches) will be excluded if they cannot refrain from using them during the two-week training period.
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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)
Allocation is computerised and so once baseline is completed participants are automatically allocated to a treatment group which the the researcher is unaware of and not involved in communicating
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomisation occurs via computerised sequence generation
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
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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
Efficacy
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Statistical methods / analysis
Multi-level modelling will be utilised to assess primary and secondary outcomes
Hierarchical regressions will be utilised to assess mediators and moderators
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Recruitment
Recruitment status
Stopped early
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Data analysis
Data collected is being analysed
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Reason for early stopping/withdrawal
Other reasons/comments
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Other reasons
we reached the required sample size for adequate power earlier than anticipated due to less attrition and greater adherence to the protocol than anticipated
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Date of first participant enrolment
Anticipated
21/02/2017
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Actual
22/02/2017
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Date of last participant enrolment
Anticipated
3/09/2018
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Actual
29/07/2017
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Date of last data collection
Anticipated
17/12/2018
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Actual
22/12/2017
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Sample size
Target
150
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Accrual to date
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Final
110
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Recruitment in Australia
Recruitment state(s)
VIC
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Deakin University, School of Psychology
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Address [1]
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School of Psychology
Faculty of Health
Deakin University
221 Burwood Highway
Burwood, VIC 3125
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Associate Professor Petra Staiger
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Address
School of Psychology
Faculty of Health
Deakin University
221 Burwood Highway
Burwood, VIC 3125
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Dr Melissa Hayden
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Address [1]
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School of Psychology
Faculty of Health
Deakin University
221 Burwood Highway
Burwood, VIC 3125
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Country [1]
294337
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Australia
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Secondary sponsor category [2]
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Individual
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Name [2]
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Karen Guo
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Address [2]
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School of Psychology
Deakin University
221 Burwood highway
Burwood Campus
Burwood 3125
Victoria
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Country [2]
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Australia
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Secondary sponsor category [3]
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Individual
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Name [3]
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Laura Hughes
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Address [3]
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School of Psychology
Deakin University
221 Burwood highway
Burwood Campus
Burwood 3125
Victoria
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Country [3]
294493
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Australia
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Secondary sponsor category [4]
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Individual
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Name [4]
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Jason Bos
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Address [4]
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School of Psychology
Deakin University
221 Burwood highway
Burwood Campus
Burwood 3125
Victoria
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Country [4]
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Australia
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Secondary sponsor category [5]
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Individual
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Name [5]
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Dr Natalia Lawrence
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Address [5]
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School of Psychology
University of Exeter
Exeter
EX4 4QG
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Country [5]
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United Kingdom
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Other collaborator category [1]
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Individual
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Name [1]
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Professor Ben Richardson
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Address [1]
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Cairnmillar Institute
993 Burke Rd
Camberwell, 3124
Victoria
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Country [1]
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Australia
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Other collaborator category [2]
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Individual
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Name [2]
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Professor Ron Borland
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Address [2]
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Cancer Council of Victoria
615 St Kilda Road
Melbourne, 3004
Victoria
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Country [2]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Deakin University Human Research Ethics Committee
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Ethics committee address [1]
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Human Research Ethics Office Deakin Research Integrity Deakin University 221 Burwood Hwy Burwood, VIC 3125
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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23/11/2015
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Approval date [1]
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22/02/2016
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Ethics approval number [1]
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2015-298
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Summary
Brief summary
Despite the supports and treatments available to assist smoking cessation, relapse remains high amongst smokers who attempt to quit. An important factor that has been identified to contribute to relapse is difficulties with impulse control, also known as response inhibition. Smokers have been found to exhibit reduced response inhibition, that is, difficulties inhibiting an automatic response such as smoking, Difficulties with response inhibition has been hypothesised to be a predictor of relapse following a quit attempt. Therefore, it would be beneficial to target response inhibition during this time period to assist in achieving and maintaining abstinence. While response inhibition interventions have not yet been investigated in smokers, other studies have found it to be effective in changing unhealthy behaviours in heavy drinkers, dieters and overweight adults. This Randomised Controlled Trial aims to investigate whether response inhibition training is effective for reducing smoking in those who are dependent on nicotine, It will also examine how a number of mediators and moderators. Our research group is collaborating with Dr Natalia Lawrence to adapt her program which was developed and evaluated in the UK in relation to food inhibition training. Participants will be allocated to either a treatment group or an active control group. The response inhibition group will complete two weeks of the smoking response inhibition training program, while the control group will complete a general response inhibition training program. All participants will complete fourteen online training sessions over a two-week period and will provide follow-up data relating to their smoking status three time points after they have completed the training - post intervention, one and three month follow up.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Petra Staiger
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Address
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School of Psychology
Faculty of Health
Deakin University
221 Burwood Highway
Burwood VIC 3125
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Country
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Australia
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Phone
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+61 3 9244 6876
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Petra Staiger
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Address
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School of Psychology
Faculty of Health
Deakin University
221 Burwood Highway
Burwood VIC 3125
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Country
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Australia
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Phone
63875
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+61 3 9244 6876
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Fax
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Email
63875
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[email protected]
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Contact person for scientific queries
Name
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Petra Staiger
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Address
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School of Psychology
Faculty of Health
Deakin University
221 Burwood Highway
Burwood VIC 3125
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Country
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Australia
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Phone
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+61 3 9244 6876
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Fax
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Email
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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
A randomized controlled trial of inhibitory control training for smoking cessation and reduction.
2019
https://dx.doi.org/10.1037/ccp0000424
N.B. These documents automatically identified may not have been verified by the study sponsor.
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