The Use of TDCS for Vaping Reduction

Center for Addiction and Mental Health (CAMH)

Status: Not yet enrolling

Conditions: Addiction; Vaping; Transcranial Direct Current Stimulation(tDCS)

Treatments: Device: Active tDCS; Device: Sham tDCS

Study type: Interventional

Funder types: Other

Identifiers

NCT06885606

007/2023

Details and patient eligibility

About

Project Summary - tDCS for Vaping Reduction

Background: While the prevalence of tobacco smoking has plateaued over the last several years, the prevalence of nicotine vaping (e-cigarettes) continues to increase exponentially in Canada. Originally touted as a safe alternative to smoking, e-cigarette use or vaping is now most popular among youth and young adults. The high prevalence of e-cigarette use, coupled with growing evidence of associated harms and reports of addiction and difficulties in quitting reinforces the urgent need to develop and test methods to attenuate e-cigarette craving as a step towards developing approaches to vaping cessation that are brief, inexpensive and effective. Non-invasive brain stimulation techniques have become a popular area of research as a treatment option for substance use disorders with growing evidence of their effectiveness for a variety of addictions. One of these techniques, transcranial direct current stimulation (tDCS), has been shown to decrease cigarette craving and consumption. Thus, the purpose of this pilot study is to evaluate the effectiveness of using tDCS for vaping reduction in e-cigarette users.

Methods: This will be a double-blind sham-controlled randomized trial whereby 40 daily nicotine-containing e-cigarette users will be recruited to undergo 10 consecutive daily sessions of tDCS (Monday to Friday for 2 weeks). Participants will be randomized (1:1) to either sham (0mA) or active tDCS (2mA), with the anode at the left dorsolateral prefrontal cortex (DLPFC) and cathode at the right DLPFC. The primary outcome is vaping frequency (puffs/day and nicotine pods/week) at end of treatment (2 weeks). The secondary outcome will be e-cigarette craving. Participants will be followed-up via the phone at 1 month and 3 months post randomization respectively.

Implication: This will be the first treatment study to target vaping reduction. There are currently no established treatment options for e-cigarette addiction and medications traditionally used for smoking cessation only address withdrawal symptoms and not addiction pathology. Thus, findings from this study may be used to inform future designs of vaping reduction strategies or vaping cessation.

Enrollment: 40 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• The participant must meet all of the inclusion criteria to be eligible for this research study:

  1. Be able to provide informed written consent
  2. Stated willingness to comply with all study procedures
  3. Age 18 - 65 years
  4. Is a daily regular use of nicotine-containing e-cigarette for at least the past 6 months
  5. Is willing to attend daily appointments for tDCS for two consecutive weeks (Monday through Friday)
  6. Is not interested in or planning to quit vaping in the next 30 days.

Exclusion criteria

• An individual who meets any of the following criteria will be excluded from participation in this research study:

  1. Substance use disorder (other than nicotine dependence) (M.I.N.I. SCID) (confirmed with urine drug screen)
  2. Current regular use of tobacco cigarettes, nicotine replacement therapy or other medications for smoking cessation
  3. Unstable psychiatric condition
  4. Recent clinically significant head trauma*
  5. History of seizures and/or epilepsy*
  6. Pacemakers or implanted electrical devices such as cochlear implants*
  7. Metal embedded in the skull*
  8. Skin lesions, open wounds, bruising, or similar injuries on the scalp*

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

40 participants in 2 patient groups

Active tDCS stimulation group

Active Comparator group

Treatment:

Device: Active tDCS

Sham tDCS stimulation group

Sham Comparator group

Description:

Sham tDCS applies a 2mA current for the initial 30 seconds, followed by 0 mA for the remaining 19.5 minutes to simulate active tDCS stimulation. The cathode electrode is placed on the right dorsolateral prefrontal cortex (DLPFC), and the anode is positioned on the left DLPFC, aligned with the electrode placement used in active tDCS.

Treatment:

Device: Sham tDCS