RecruitingAlcohol Use Disorder
A Combined Neurofeedback-TMS Intervention for Alcohol Use Disorder
Eligible age
19–65 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
See if you qualify for this study
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About this study
The goal of this clinical study is to test the effectiveness of a supplemental fMRI neurofeedback and/or TMS intervention in individuals seeking treatment for Alcohol Use Disorder. After an initial visit, participants will come in once a week for four (4) weeks for an intervention session, which may or may not include TMS and MRI. Participants will be contacted for monthly follow-ups (remotely) for up to 12 months and will be asked to come in for two MRI follow-ups at 6 and 12 months.
Sponsor: Auburn University
You may qualify if…
- ✓ 1. Age 19-65
- ✓ 2. Receiving treatment for Alcohol Use Disorder
You may not qualify if…
- ✕ 1. MRI Contraindications
- ✕ 1. Presence of metal in the body that would make having a 7T MRI unsafe (including facial tattoos)
- ✕ 2. Claustrophobia, such that individual would be unable to stay in the MRI for up to 1 hr
- ✕ 3. Hearing loss, including tinnitus, that might be made worse by MRI or TMS
- ✕ 2. TMS Contraindications
- ✕ 1. Has ever had a seizure, or has a family history of epilepsy
- ✕ 2. Taking medications or substances that lower the seizure threshold
- ✕ 3. Implanted devices that are in the head or rely on physiological signals
Where it's recruiting
Alabama
Auburn
Source: ClinicalTrials.gov · NCT05621538 · last updated 2025-10-07