Combining Noninvasive Brain Stimulation and Cognitive Training on Tobacco Craving
Not Applicable
- Conditions
- Tobacco Use Disorder
- Interventions
- Behavioral: Cognitive trainingDevice: Noninvasive brain stimulation (active)Device: Noninvasive brain stimulation (sham)
- Registration Number
- NCT02810574
- Lead Sponsor
- Laval University
- Brief Summary
The purpose of this study is to determine whether combining noninvasive brain stimulation with cognitive training can reduce craving in adults with tobacco use disorder.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
- 20-60 years old
- Smoking > 15 cigarettes per day
- Tobacco Use Disorder according to Diagnostic and Statistical Manual V criteria
Exclusion Criteria
- Contraindications to noninvasive brain stimulation
- Psychiatric or neurologic condition
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Active noninvasive brain stimulation and cognitive training Cognitive training In active condition, subject will receive stimulation during all the 30-minute stimulation period combined with cognitive training. Active noninvasive brain stimulation and cognitive training Noninvasive brain stimulation (active) In active condition, subject will receive stimulation during all the 30-minute stimulation period combined with cognitive training. Sham noninvasive brain stimulation Noninvasive brain stimulation (sham) In sham condition, subject will receive stimulation only during the first 30 seconds of the 30-minute stimulation period combined with cognitive training. Sham noninvasive brain stimulation Cognitive training In sham condition, subject will receive stimulation only during the first 30 seconds of the 30-minute stimulation period combined with cognitive training.
- Primary Outcome Measures
Name Time Method Changes in tobacco craving assessed by the Questionnaire of Smoking Urge immediately before and immediately after the end of the noninvasive brain stimulation
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Centre Interdisciplinaire de Recherche en Réadaptation et Intégration
🇨🇦Quebec, Canada