Tobacco Retraining of Automatic Approach to Treat Individuals With Tobacco Dependence and Severe Concurrent Disorders.
- Conditions
- Tobacco Retraining of Automatic ApproachPlacebo Task
- Interventions
- Behavioral: TRAA intervention
- Registration Number
- NCT01902199
- Lead Sponsor
- University of British Columbia
- Brief Summary
A randomized control trial evaluating a novel smoking cessation intervention in individuals at a an inpatient clinic for clients with addiction and concurrent disorders. The intervention is based on cognitive bias modification, where participants are explicitly or implicitly trained to make avoidance movements by pushing a joystick in response to pictures of smoking, and as a result altering their cognitive biases towards smoking and tobacco dependence.
Hypothesis: Participation in the experimental (tobacco-avoidance) condition will induce reduction of smoking, assessed as lower levels of carbon monoxide measured at baseline and 12 week follow-up.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
- Proficiency to read and write english
- A minimum score of 5 or higher on the fagerström test for nicotine dependence, indicating a medium dependence
- Current smoking will be validated by Carbon monoxide breath monitor
- Patients not yet stabilized enough to allow for regular participation in the intervention
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description TRAA TRAA intervention participants will be given the active TRAA intervention where landscape images are linked with a push motion, and portrait images linked with a pull motion. Pictures will exclusively be related to smoking. Control TRAA intervention participants will be given a mix of landscape and portrait pictures, equally divided into push or pull. the images will be a mix of smoking related pictures and non smoking pictures.
- Primary Outcome Measures
Name Time Method Carbon monoxide levels in breath baseline, 12 weeks The breath carbon monoxide monitoring device will be used both before the intervention for a baseline measure and at the 12-week follow-up for comparison. These two measurements will be used to detect changes in smoking patterns that may have occurred during this interval. The method allows to objectify abstinence from smoking.
- Secondary Outcome Measures
Name Time Method Fagerström test for Nicotine dependence (FTND) Baseline The FTND is a 6-item questionnaire scored to test level of nicotine dependence, and will be presented to patients prior to the intervention. Patients meeting a cut-off score of 5 or higher will be eligible to participate in the intervention portion of this study.
Trial Locations
- Locations (1)
Burnaby Centre for Mental Health and Addiction
🇨🇦Burnaby, British Columbia, Canada