Combining rTMS With Varenicline to Prevent Smoking Lapse in Schizophrenia
Tobacco Use Disorder, Schizophrenia, Cognitive Functioning
About this trial
This is an interventional treatment trial for Tobacco Use Disorder focused on measuring Schizophrenia, Smoking, Lapse, Varenicline, Sham Repetitive Transcranial Magnetic Stimulation (rTMS)
Eligibility Criteria
Inclusion Criteria:
- smokers with schizophrenia, non-treatment seeking (i.e., not trying to quit as indicated by <7 on the contemplation ladder)
- ages 18-55
- IQ ≥80 on the Weschler Test of Adult Reading
- Fagerstrom Test for Nicotine Dependence (FTND) ≥5
- smoke ≥ 10 cigarettes per day
- must meet SCID for DSM-5 diagnosis criteria for schizophrenia
- must be in stable remission from positive symptoms of psychosis as judged by a PANSS positive score total score <70
- must be receiving a stable dose of antipsychotics for >1month.
Exclusion Criteria:
- substance use (except nicotine or caffeine) in the last month
- a history of alcohol/drug abuse in the 3 months before study enrolment and use of opioids (e.g., meperidine, oxycodone, methadone)
- current use of smoking cessation aids (e.g., nicotine replacement therapy, bupropion or varenicline)
- pregnancy or nursing
- a history of renal insufficiency or a hypersensitivity to varenicline (Chantix®)
- a history of neurological illness like epilepsy or medical condition known to significantly influence neurocognitive function, at the discretion of the PI
- any other medical condition deemed relevant by the PI
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Sham Comparator
Active rTMS (20Hz)
Sham rTMS
Active rTMS administered with the MagProX100/R30 stimulator equipped with the B65 active coil for dorsolateral prefrontal cortex (DLPFC) stimulator (MagVenture, Farum, Denmark).The randomization order will be determined by a project scientist from Temerty. While the primary aim of this study is not to treat individuals with tobacco dependence, it is imperative that participants attend weekly study visits in an attempt to achieve end of study (Day 28) tobacco abstinence.
Sham rTMS administered with the MagProX100/R30 stimulator equipped with the B65 placebo coil for DLPFC stimulator (MagVenture, Farum, Denmark). The randomization order will be determined by a project scientist from Temerty. While the primary aim of this study is not to treat individuals with tobacco dependence, it is imperative that participants attend weekly study visits in an attempt to achieve end of study (Day 28) tobacco abstinence.