Actively Recruiting

Phase 2
Age: 18Years +
All Genders
ID07292883

Accelerated Deep Transcranial Magnetic Stimulation for Smoking Cessation

Led by Waypoint Centre for Mental Health Care · Updated on 2026-04-21

40

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating whether a 5-day course of bilateral accelerated deep transcranial magnetic stimulation (aTMS) can be a feasible treatment to help adults aged 18 to 65 with Tobacco Use Disorder quit smoking. This Phase 2 clinical trial aims to enroll 30 to 40 participants and will assess treatment tolerability, acceptability, participant retention, and adherence to the scheduled sessions. It also explores how aTMS affects smoking outcomes such as abstinence, craving, cigarette consumption, and dependence severity over several weeks of follow-up. The treatment involves bilateral accelerated repetitive transcranial magnetic stimulation targeting the insula and prefrontal cortex using the Health Canada-approved H4 coil. Participants will receive 20 sessions of aTMS over five consecutive days, with four sessions each day. This accelerated approach differs from traditional methods by delivering multiple sessions daily. The study focuses on the feasibility and tolerability of this intensive 1-week treatment schedule. Participants will attend treatment sessions daily for one week, followed by follow-up visits at weeks 3, 5, 9, 13, and 26 to monitor smoking abstinence and other outcomes. Researchers will collect data on side effects, treatment acceptability, session attendance, and changes in tobacco craving and dependence. The study carefully monitors participant safety and retention throughout the treatment and follow-up periods, aiming to understand the potential of aTMS in supporting smoking cessation over six months.

CONDITIONS

Brief Title

Accelerated dTMS Smoking Cessation

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 years or older
  • Diagnosed with Tobacco Use Disorder according to DSM-5
  • Fagerstrom Test of Nicotine Dependence score of 4 or higher
  • Motivated to quit smoking within 30 days with a Contemplation Ladder score of 7 or more
  • Able and willing to sign informed consent
  • Willing to comply with all study procedures
  • Able to communicate in English
Not Eligible

You will not qualify if you...

  • Not smoked for 3 months before screening
  • Currently using other smoking cessation aids
  • Contraindication to repetitive transcranial magnetic stimulation (rTMS)
  • Pregnant, trying to become pregnant, or breastfeeding
  • History of cerebrovascular disease
  • Unstable major psychiatric disorders preventing study participation
  • Serious neurological or medical conditions preventing inclusion
  • Personal or family history of seizures
  • Taking medications that lower seizure threshold such as clozapine
  • Using more than 2 mg lorazepam daily or any anticonvulsant medication

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - 5 days

Participants receive accelerated bilateral deep repetitive transcranial magnetic stimulation targeting the insula and prefrontal cortex using the H4 coil over five consecutive days.

4 sessions daily for 5 consecutive days

Follow-up

Duration - Up to 26 weeks

Participants are monitored for smoking abstinence and related outcomes following treatment completion.

Visits occurring periodically during follow-up

Trial Site Locations

Total: 2 locations

1

Waypoint Centre for Mental Health Care

Penetanguishene, Ontario, Canada

Actively Recruiting

2

Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada

Not Yet Recruiting

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Research Team

F

Florence Tang, MA

V

Vincent Wang, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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