rTMS Effects on Smoking Cessation and Cognition in Schizophrenia

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Tony George, Centre for Addiction and Mental Health
ClinicalTrials.gov Identifier:
NCT00736710
First received: August 15, 2008
Last updated: December 4, 2012
Last verified: December 2012

August 15, 2008
December 4, 2012
December 2008
May 2011   (final data collection date for primary outcome measure)
Smoking abstinence (7-day point prevalence) at trial endpoint (Days 63-70) as assessed by self-reported smoking abstinence plus Expired Breath Carbon Monoxide Level <10ppm. [ Time Frame: trial endpoint ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00736710 on ClinicalTrials.gov Archive Site
  • P50/NI, N-Back and VSWM Working Memory Performance [ Time Frame: intermittent ] [ Designated as safety issue: No ]
  • Expired Breath Carbon Monoxide Levels [ Time Frame: intermittent ] [ Designated as safety issue: No ]
  • Tobacco Craving (Tiffany QSU) and Withdrawal (Minnesota NMS) [ Time Frame: intemittent ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
rTMS Effects on Smoking Cessation and Cognition in Schizophrenia
Effects of rTMS on Smoking Cessation and Cognitive Outcomes in Outpatients With Schizophrenia Treated With Transdermal Nicotine Patch

Patients with schizophrenia have high rates of cigarette smoking and tobacco dependence, and great difficulties in quitting smoking. The development of novel and more effective treatments for tobacco dependence in this population is thus needed. This study will test the hypothesis that repetitive transcranial magnetic stimulation (rTMS) may facilitate smoking cessation with the transdermal nicotine patch (TNP) in patients with schizophrenia motivated to quit smoking. A total of N=40 smokers with schizophrenia would be assigned to either active rTMS (N=20) or sham rTMS (N=20) as a treatment regimen of 5X/week treatments for four weeks. All subjects would receive TNP (21 mg/24h) and weekly group behavioral therapy for smoking cessation for a total of 10 weeks. The investigators predict that active rTMS will be well-tolerated and superior to sham rTMS for enhancing smoking cessation rates in smokers with schizophrenia.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
  • Cigarette Smoking
  • Schizophrenia
  • Procedure: Repetitive Transcranial Magnetic Stimulation (rTMS)
    The rTMS procedures will be delivered in a single-blind fashion by the rTMS technician at the CAMH rTMS Laboratory. All subjects would be enrolled in a 10-week smoking cessation program using weekly group behavioral therapy which will emphasize psychoeducation about the effects of smoking on psychiatric and medical aspects of schizophrenia, social skills training, relapse-prevention skills training and benefits of quitting smoking. All subjects would start group therapy interventions in Week 1 of the trial, and begin rTMS procedures in a separate session on Week 2. The transdermal nicotine patch (TNP; 21 mg/24h) would be applied during the quit date at Week 3 (Day 15). At the end of the 10-week trial, TNP and group therapy would be discontinued.
  • Procedure: Sham Repetitive Transcranial Magnetic Stimulation (rTMS)
    The rTMS procedures will be delivered in a single-blind fashion by the rTMS technician at the CAMH rTMS Laboratory. All subjects would be enrolled in a 10-week smoking cessation program using weekly group behavioral therapy which will emphasize psychoeducation about the effects of smoking on psychiatric and medical aspects of schizophrenia, social skills training, relapse-prevention skills training and benefits of quitting smoking. All subjects would start group therapy interventions in Week 1 of the trial, and begin rTMS procedures in a separate session on Week 2. The transdermal nicotine patch (TNP; 21 mg/24h) would be applied during the quit date at Week 3 (Day 15). At the end of the 10-week trial, TNP and group therapy would be discontinued.
  • Experimental: 1
    Intervention: Procedure: Repetitive Transcranial Magnetic Stimulation (rTMS)
  • Sham Comparator: 2
    Intervention: Procedure: Sham Repetitive Transcranial Magnetic Stimulation (rTMS)
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
15
May 2011
May 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • DSM-IV diagnosis of schizophrenia or schizoaffective disorder
  • Smoking at least 10 cigarettes per day and a Fagerstrom score of at least 4.
  • Willing to quit smoking in the next 30 days.

Exclusion Criteria:

  • Active alcohol or illicit drug abuse or dependence in the past 3 months
  • A history of seizures, head trauma or space occupying lesions.
  • A history of alcohol or illicit drug abuse in the past 6 months.
  • Intolerance of the nicotine patch or its excipients
  • Evidence for psychiatric instability as judged by acute psychotic exacerbations, suicidal or homicidal ideation.
  • Females who are pregnant.
Both
18 Years to 60 Years
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT00736710
121/2007
No
Tony George, Centre for Addiction and Mental Health
Centre for Addiction and Mental Health
Not Provided
Principal Investigator: Tony George, MD Centre for Addiction and Mental Health
Centre for Addiction and Mental Health
December 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP