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Clinical Trials/NCT02810574
NCT02810574UnknownNot Applicable

Combining Noninvasive Brain Stimulation and Cognitive Training on Tobacco Craving

Laval University1 site in 1 country24 target enrollmentStarted: March 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
24
Locations
1
Primary Endpoint
Changes in tobacco craving assessed by the Questionnaire of Smoking Urge

Study Overview

Brief Summary

The purpose of this study is to determine whether combining noninvasive brain stimulation with cognitive training can reduce craving in adults with tobacco use disorder.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Triple (Participant, Care Provider, Outcomes Assessor)

Eligibility Criteria

Ages
20 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • 20-60 years old
  • Smoking > 15 cigarettes per day
  • Tobacco Use Disorder according to Diagnostic and Statistical Manual V criteria

Exclusion Criteria

  • Contraindications to noninvasive brain stimulation
  • Psychiatric or neurologic condition

Arms & Interventions

Active noninvasive brain stimulation and cognitive training

Active Comparator

In active condition, subject will receive stimulation during all the 30-minute stimulation period combined with cognitive training.

Intervention: Cognitive training (Behavioral)

Active noninvasive brain stimulation and cognitive training

Active Comparator

In active condition, subject will receive stimulation during all the 30-minute stimulation period combined with cognitive training.

Intervention: Noninvasive brain stimulation (active) (Device)

Sham noninvasive brain stimulation

Sham Comparator

In sham condition, subject will receive stimulation only during the first 30 seconds of the 30-minute stimulation period combined with cognitive training.

Intervention: Cognitive training (Behavioral)

Sham noninvasive brain stimulation

Sham Comparator

In sham condition, subject will receive stimulation only during the first 30 seconds of the 30-minute stimulation period combined with cognitive training.

Intervention: Noninvasive brain stimulation (sham) (Device)

Outcomes

Primary Outcomes

Changes in tobacco craving assessed by the Questionnaire of Smoking Urge

Time Frame: immediately before and immediately after the end of the noninvasive brain stimulation

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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