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Clinical Trials/NCT03841292
NCT03841292
Completed
Not Applicable

Using Non-invasive Brain Stimulation (tDCS) to Improve the Effectiveness of Varenicline for Treating Tobacco Dependence: a Randomized Controlled Trial

Centre for Addiction and Mental Health1 site in 1 country41 target enrollmentOctober 1, 2018

Overview

Phase
Not Applicable
Intervention
Varenicline
Conditions
Tobacco Dependence
Sponsor
Centre for Addiction and Mental Health
Enrollment
41
Locations
1
Primary Endpoint
Change in smoking status over time
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The addition of tDCS as an adjunct to pharmacotherapy is a novel approach but one that is grounded in a growing evidence-base.The primary objective of this research is to provide preliminary evidence of the effectiveness of tDCS as an adjunct treatment to pharmacotherapy for smoking cessation. The investigators hypothesize that the addition of active tDCS to the left DLPFC will improve the effectiveness of varenicline as reflected by higher quit rates at end of treatment compared to the sham group. Smoking status will be biochemically confirmed at various time points using expired cotinine measures. Furthermore, the investigators will be collecting neuroimaging (fMRI) data as well as measures of attentional bias to explore the neurological and physiological correlates from using adjunct tDCS and varenicline therapy.

Detailed Description

While varenicline on its own is the most effective medication for smoking cessation, long-term abstinence is still relatively poor. The primary objective of this study is to evaluate the effectiveness of adjunct active tDCS with varenicline in treating tobacco dependence. This study is a double-blind, sham-controlled, randomized clinical trial where 50 daily dependent treatment seeking smokers will be recruited at the Nicotine Dependence Clinic in Toronto, Canada. Participants will be receiving twelve weeks of varenicline treatment (1mg b.i.d.) and randomized 1:1 to either active tDCS (active: 20 minutes at 2 mA) or sham tDCS (30 seconds at 2 mA, 19.5 minutes at 0 mA), daily (M-F) for the first 2 weeks and then every 2 weeks for the next 10 weeks. There will be 2 fMRI scans at baseline and 1 scan at end-of-treatment. Eye-tracking viewing tests will be conducted at baseline, weeks 4, 8, 12 and at 6 months follow up. During the 6 month follow-up, participants will be answering questions regarding their smoking behaviour and craving. Smoking status will be biochemically confirmed at each study visit using expired cotinine.

Registry
clinicaltrials.gov
Start Date
October 1, 2018
End Date
January 31, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Laurie Zawertailo

Senior Scientist

Centre for Addiction and Mental Health

Eligibility Criteria

Inclusion Criteria

  • Male or Female
  • Aged 19-65
  • Treatment seeking smoker
  • Daily smoker of CPD\>8
  • Able to attend daily appointments for tDCS for the first 2 weeks and booster sessions for the next 10 weeks.
  • Wiling to undergo 3 fMRI sessions

Exclusion Criteria

  • Current/recent DSM-IV Axis I diagnosis
  • Current use of psychoactive drugs or medications
  • History of seizures/epilepsy
  • Current use of NRT, e-cigarettes or other medications for smoking cessation
  • Metal embedded in skull or implanted electrical devices
  • No head injury (concussion or loss of consciousness for more than an hour)
  • Contraindications to fMRI
  • Contraindications to varenicline

Arms & Interventions

Active tDCS+Varenicline

Active 2mA tDCS (Nuraleve, Canada) with the anode placed over the left dorsolateral prefrontal cortex (dlPFC) and the cathode placed over the right dlPFC for 20 minutes per session. Daily stimulation between Monday to Friday for the first two weeks and then booster sessions every other week for the next 10 weeks.

Intervention: Varenicline

Active tDCS+Varenicline

Active 2mA tDCS (Nuraleve, Canada) with the anode placed over the left dorsolateral prefrontal cortex (dlPFC) and the cathode placed over the right dlPFC for 20 minutes per session. Daily stimulation between Monday to Friday for the first two weeks and then booster sessions every other week for the next 10 weeks.

Intervention: Active tDCS

Sham tDCS+Varenicline

Sham tDCS (Nuraleve, Canada)(30 seconds of 2mA and 19.5 minutes of 0 mA) with the anode placed over the left dorsolateral prefrontal cortex (dlPFC) and the cathode placed over the right dlPFC for 20 minutes per session. Daily stimulation between Monday to Friday for the first two weeks and then booster sessions every other week for the next 10 weeks.

Intervention: Varenicline

Sham tDCS+Varenicline

Sham tDCS (Nuraleve, Canada)(30 seconds of 2mA and 19.5 minutes of 0 mA) with the anode placed over the left dorsolateral prefrontal cortex (dlPFC) and the cathode placed over the right dlPFC for 20 minutes per session. Daily stimulation between Monday to Friday for the first two weeks and then booster sessions every other week for the next 10 weeks.

Intervention: Sham tDCS

Outcomes

Primary Outcomes

Change in smoking status over time

Time Frame: At weeks 12 and 26 following start of treatment

30 Day Continuous abstinence confirmed by expired CO \</= 4 ppm

Secondary Outcomes

  • Change in functional brain activation during cognitive tasks(At baseline and 12 weeks following start of treatment)
  • Change in preference of attention towards visual cues(At weeks 4,8, 12 and 26 weeks following start of treatment.)

Study Sites (1)

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