Skip to main content
Clinical Trials/NCT01902199
NCT01902199
Withdrawn
Not Applicable

Studying a Novel Intervention, the Tobacco Retraining of Automatic Approach (TRAA), to Treat Individuals With Tobacco Dependence and Severe Concurrent Disorders

University of British Columbia1 site in 1 countryOctober 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tobacco Retraining of Automatic Approach
Sponsor
University of British Columbia
Locations
1
Primary Endpoint
Carbon monoxide levels in breath
Status
Withdrawn
Last Updated
4 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
December 2015
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christian Schutz

Dr. Christian Schutz

University of British Columbia

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • Patients not yet stabilized enough to allow for regular participation in the intervention

Outcomes

Primary Outcomes

Carbon monoxide levels in breath

Time Frame: 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 Outcomes

  • Fagerström test for Nicotine dependence (FTND)(Baseline)

Study Sites (1)

Loading locations...

Similar Trials