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Combining rTMS With Varenicline to Prevent Smoking Lapse in Schizophrenia

Primary Purpose

Tobacco Use Disorder, Schizophrenia, Cognitive Functioning

Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Active rTMS (20Hz)
Sham rTMS
Sponsored by
Centre for Addiction and Mental Health
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

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

    Arm Type

    Experimental

    Sham Comparator

    Arm Label

    Active rTMS (20Hz)

    Sham rTMS

    Arm Description

    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.

    Outcomes

    Primary Outcome Measures

    Time to Smoking Lapse (TTL)
    A measure of ability to resist smoking lapse during a 50 minute ad lib cigarette smoking period at Day 28 of the trial in SWS. Higher values indicate increased ability to resist smoking lapse.

    Secondary Outcome Measures

    Smoking Topography
    Using the Clinical Research Support System (CReSS), the investigators will assess smoking reinforcement outcomes including total number of puffs smoked per session, total puff volume per cigarette, puffs per cigarette, duration of inter--puff interval, average maximum puff velocity, average puff volume and average puff duration.
    Spatial Delayed Response (SDR)/Visuospatial Working Memory (VSWM) Task
    Subjects focus on a central fixation cross on a computer screen, a dot--shaped cue flashes towards the outer edge of the screen. A delay period then occurs, during which a series of shapes flash in the center of the screen;; the subjects must respond on the spacebar when the diamond shape appears. After the delay, which ranges from 5--30s to assess shorter-- vs. longer--term VSWM, the fixation cross returns and the subject must indicate where they remember seeing the dot. Results are reported as the averaged "distance from target" (cm) for the 16 trials at each delay condition. Duration: 15 minutes

    Full Information

    First Posted
    March 29, 2018
    Last Updated
    September 1, 2023
    Sponsor
    Centre for Addiction and Mental Health
    Collaborators
    Yale University, Oregon State University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03497299
    Brief Title
    Combining rTMS With Varenicline to Prevent Smoking Lapse in Schizophrenia
    Official Title
    Combining rTMS With Varenicline to Prevent Smoking Lapse in Schizophrenia
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2023
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    lack of funding
    Study Start Date
    July 1, 2018 (Anticipated)
    Primary Completion Date
    August 31, 2022 (Anticipated)
    Study Completion Date
    August 31, 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Centre for Addiction and Mental Health
    Collaborators
    Yale University, Oregon State University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Tobacco smokers with schizophrenia are known to be resistant smokers, with high rates of smoking and inability to quit in the long-term, often related to smoking relapse. This may relate to problems with frontal lobe function associated with schizophrenia, which make these patients have great difficulty in dealing with smoking withdrawal, urges and cravings. The current study will develop a combination approach that takes advantage of brain stimulation of the frontal lobes (repetitive transcranial magnetic stimulation (rTMS), in combination with the anti-smoking drug varenicline, to prevent smoking lapse using a well-established human laboratory method. Results from this study may have important implications for developing novel treatment approaches for smokers with schizophrenia.
    Detailed Description
    Tobacco smokers with schizophrenia (SWS) represent a subset of smokers with high smoking prevalence compared to the general population, and reduced ability to quit smoking and to resist smoking relapse. There is some evidence that first-line treatments for tobacco use disorder are safe and effective for smoking cessation and smoking relapse-prevention in SWS, but these treatments do not appear to be as effective in smokers with a mental illness as compared to non-psychiatric tobacco smokers. Novel approaches to identify safe and effective treatments using human laboratory models may be an efficient strategy towards this important clinical goal. The proposed human laboratory study will test the effects of standard pharmacotherapy for tobacco use disorder, the nicotinic partial agonist varenicline, in combination with an established brain stimulation method (repetitive transcranial magnetic stimulation;; rTMS) in SWS. This will allow for the determination of the benefits of combining rTMS with varenciline in SWS using a validated smoking lapse paradigm developed by the collaborator Sherry McKee, Ph.D. at Yale University. The present study represents a novel neuroscience-based strategy for targeting dorsolateral prefrontal cortex (DLPFC) dysfunction in schizophrenia, and is consistent with a target engagement and validation approach as endorsed by NIDA/NIH. Moreover, the subject population the investigators are targeting (SWS) are prone to quit attempt failures and rapid relapse to tobacco smoking, and are in need of novel and effective anti-smoking lapse interventions. The investigators' preliminary data support the use of the combination of varenicline and high-frequency (20 Hz) rTMS to target smoking lapse and craving outcomes in SWS. Accordingly, the investigators believe that the proposed goals, approach and implications for treatment development are substantial and likely to impact positively on clinical treatment research outcomes in this marginalized population of tobacco smokers. Specifically, using a randomized, double-blind, placebo-controlled parallel groups experimental design, the investigators will determine whether the combination of varenicline (2 mg/day) and high-frequency (20 Hz) rTMS versus varenicline and sham rTMS directed to the DLPFC will be superior for the prevention of tobacco smoking lapse behaviors in cigarette smokers with schizophrenia (N=80). Hypothesis 1 (H1): Active (20 Hz) versus Sham rTMS will increase the time to smoking lapse in combination with varenicline in SWS. Hypothesis 2 (H2): Active (20 Hz) versus Sham rTMS will improve prefrontal cognition in SWS, and this will be associated with increased ability to resist smoking lapse.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Tobacco Use Disorder, Schizophrenia, Cognitive Functioning, Craving
    Keywords
    Schizophrenia, Smoking, Lapse, Varenicline, Sham Repetitive Transcranial Magnetic Stimulation (rTMS)

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Model Description
    The study is a randomized controlled trial of active versus sham high frequency rTMS to the dorsolateral prefrontal cortex (DLPFC) in patients with schizophrenia who have co-occurring tobacco use disorder. The duration of treatment is 4 weeks and all subjects would receive open label Varenicline 2mg/day. The primary outcome measure is time to lapse to smoking.
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Masking Description
    The investigators will have a sham rTMS coil to provide full blinding for the active rTMS condition.
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Active rTMS (20Hz)
    Arm Type
    Experimental
    Arm Description
    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.
    Arm Title
    Sham rTMS
    Arm Type
    Sham Comparator
    Arm Description
    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.
    Intervention Type
    Device
    Intervention Name(s)
    Active rTMS (20Hz)
    Intervention Description
    Repetitive Transcranial Magnetic Stimulation (rTMS) Procedures: On Day 1, participants will be randomly assigned to receive active or sham rTMS using the MagProX100/R30 stimulator equipped with the B65 active/ placebo coil for DLPFC stimulator (MagVenture, Farum, Denmark) for a period of 28 days.
    Intervention Type
    Device
    Intervention Name(s)
    Sham rTMS
    Intervention Description
    Repetitive Transcranial Magnetic Stimulation (rTMS) Procedures: On Day 1, participants will be randomly assigned to receive active or sham rTMS using the MagProX100/R30 stimulator equipped with the B65 active/ placebo coil for DLPFC stimulator (MagVenture, Farum, Denmark) for a period of 28 days.
    Primary Outcome Measure Information:
    Title
    Time to Smoking Lapse (TTL)
    Description
    A measure of ability to resist smoking lapse during a 50 minute ad lib cigarette smoking period at Day 28 of the trial in SWS. Higher values indicate increased ability to resist smoking lapse.
    Time Frame
    Day 28
    Secondary Outcome Measure Information:
    Title
    Smoking Topography
    Description
    Using the Clinical Research Support System (CReSS), the investigators will assess smoking reinforcement outcomes including total number of puffs smoked per session, total puff volume per cigarette, puffs per cigarette, duration of inter--puff interval, average maximum puff velocity, average puff volume and average puff duration.
    Time Frame
    Day 28 (in comparison to baseline results at Day 0)
    Title
    Spatial Delayed Response (SDR)/Visuospatial Working Memory (VSWM) Task
    Description
    Subjects focus on a central fixation cross on a computer screen, a dot--shaped cue flashes towards the outer edge of the screen. A delay period then occurs, during which a series of shapes flash in the center of the screen;; the subjects must respond on the spacebar when the diamond shape appears. After the delay, which ranges from 5--30s to assess shorter-- vs. longer--term VSWM, the fixation cross returns and the subject must indicate where they remember seeing the dot. Results are reported as the averaged "distance from target" (cm) for the 16 trials at each delay condition. Duration: 15 minutes
    Time Frame
    Day 28 (in comparison to baseline results at Day 0)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    55 Years
    Accepts Healthy Volunteers
    No
    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

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    29486960
    Citation
    Kozak K, Sharif-Razi M, Morozova M, Gaudette EV, Barr MS, Daskalakis ZJ, Blumberger DM, George TP. Effects of short-term, high-frequency repetitive transcranial magnetic stimulation to bilateral dorsolateral prefrontal cortex on smoking behavior and cognition in patients with schizophrenia and non-psychiatric controls. Schizophr Res. 2018 Jul;197:441-443. doi: 10.1016/j.schres.2018.02.015. Epub 2018 Feb 24.
    Results Reference
    result
    PubMed Identifier
    22464727
    Citation
    Wing VC, Bacher I, Wu BS, Daskalakis ZJ, George TP. High frequency repetitive transcranial magnetic stimulation reduces tobacco craving in schizophrenia. Schizophr Res. 2012 Aug;139(1-3):264-6. doi: 10.1016/j.schres.2012.03.006. Epub 2012 Mar 29. No abstract available.
    Results Reference
    result

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    Combining rTMS With Varenicline to Prevent Smoking Lapse in Schizophrenia

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