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Behavioural Intervention
Neurofeedback (from fMRI and/or EEG) for Nicotine Addiction
N/A
Waitlist Available
Led By R. Alison Adcock, MD, PhD
Research Sponsored by Duke University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up to occur following the neurofeedback session, up to 30 minutes following the session
Awards & highlights
Study Summary
This trial aims to see if a non-medication intervention can increase motivation for non-drug rewards (like a favorite food) for people with and without nicotine dependence.
Eligible Conditions
- Nicotine Addiction
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ collected once during the screening visit
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~collected once during the screening visit
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in reward-related brain activation
Secondary outcome measures
Dopamine availability
Onset to smoking a cigarette
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Reward-related Brain Region FeedbackExperimental Treatment1 Intervention
Participants in this group will receive neurofeedback from a reward-related brain area (e.g., VTA, PFC) using EEG and/or fMRI during the experiment.
Group II: Noise ControlPlacebo Group1 Intervention
Participants in this group will receive sham neurofeedback. Participants will be debriefed at the end of the study.
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Who is running the clinical trial?
Brain & Behavior Research FoundationOTHER
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