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Behavioural Intervention
Real TBS to the dlPFC for Alcohol Consumption
N/A
Waitlist Available
Led By Colleen Hanlon, PhD
Research Sponsored by Wake Forest University Health Sciences
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 hour after the intervention
Awards & highlights
Study Summary
This trial is looking at a new way to treat alcohol use disorder by using brain stimulation. They will be studying how well it works and if it is safe.
Eligible Conditions
- Alcohol Consumption
- Alcoholism
- Traumatic Injury
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline to 1 hour after the intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to 1 hour after the intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Ethanol
Secondary outcome measures
Neuroimaging outcomes: change in brain response to alcohol cues
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Real TBS to the dlPFCExperimental Treatment1 Intervention
One session of real intermittent Theta Burst Stimulation (TBS) will be delivered to the left dorsolateral prefrontal cortex (dlPFC)
Group II: Sham TBS to the dlPFCPlacebo Group1 Intervention
One session of sham Theta Burst Stimulation (TBS) will be delivered to the left dorsolateral prefrontal cortex (dlPFC)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Real iTBS to the dlPFC
2020
N/A
~20
Find a Location
Who is running the clinical trial?
Wake Forest University Health SciencesLead Sponsor
1,239 Previous Clinical Trials
1,004,172 Total Patients Enrolled
Colleen Hanlon, PhDPrincipal InvestigatorWake Forest University
4 Previous Clinical Trials
322 Total Patients Enrolled
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