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RECRUITING
NCT05621538
NA

A Combined Neurofeedback-TMS Intervention for Alcohol Use Disorder

Sponsor: Auburn University

View on ClinicalTrials.gov

Summary

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.

Key Details

Gender

All

Age Range

19 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

90

Start Date

2025-10-01

Completion Date

2026-03-31

Last Updated

2025-10-07

Healthy Volunteers

No

Interventions

BEHAVIORAL

Realtime fMRI Neurofeedback - Active

fMRI aided reinforcement of craving regulation

DEVICE

TMS - Active

rTMS to right dorsolateral prefrontal cortex to reduce craving

BEHAVIORAL

Realtime fMRI Neurofeedback - Yoked Sham

Display of feedback from other participant's sessions to serve as a sham for fMRI aided reinforcement of craving regulation

DEVICE

TMS - Sham

rTMS using placebo coil (no brain stimulation, emulates other features of active TMS), placed over right dorsolateral prefrontal cortex

Locations (1)

Auburn University

Auburn, Alabama, United States