Actively Recruiting

Phase 2
Age: 21Years - 60Years
All Genders
Healthy Volunteers
ID04770025

Transcranial Alternating Current Stimulation to Boost the Efficacy of Motivational Interviewing in Adults With Alcohol Use Disorder

Led by The Mind Research Network · Updated on 2025-05-08

75

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

Sponsors

T

The Mind Research Network

Lead Sponsor

N

National Institute of General Medical Sciences (NIGMS)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of transcranial alternating current stimulation (tACS) combined with motivational interviewing (MI) in people who drink alcohol at above low-risk levels. This proof-of-concept randomized clinical trial aims to test whether adding tACS during MI sessions can influence brain activity and reduce risky drinking behaviors. The study involves 75 participants with problematic drinking who are considering treatment for their alcohol use disorder. Participants are randomly assigned to one of three groups: MI with active tACS stimulation, MI with sham (placebo) stimulation, or a delayed treatment group receiving MI only without stimulation. The active and sham groups undergo brain imaging including magnetoencephalography (MEG) and MRI scans during the sessions to measure brain responses. Each MI session lasts about 30 minutes. The delayed treatment group does not receive brain imaging. During the study, all participants report their alcohol use one month after the intervention through an online assessment. Researchers monitor brain activity, alcohol and cannabis use, emotions, and risk-taking behavior. Speech during MI sessions is recorded and analyzed to ensure proper counseling techniques. The total study duration includes initial sessions, brain scans for some groups, and follow-up assessments to evaluate changes in heavy drinking days and other drinking behaviors.

CONDITIONS

Brief Title

A Pilot Study of Non-invasive Brain Stimulation to Boost the Efficacy of Psychotherapy in a Community Sample of People Who Drink Alcohol

Who Can Participate

Age: 21Years - 60Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Self-identify as having problem drinking
  • Right-handed
  • Age 21-60 years
  • AUDIT score indicating risky drinking
Not Eligible

You will not qualify if you...

  • Left-handed or ambidextrous
  • Currently engaged in treatment for alcohol use disorder
  • Received treatment for alcohol use disorder within the prior 12 months
  • History of brain injury or neurological diagnosis
  • Evidence of current psychosis
  • Past-year substance use disorder other than alcohol, marijuana, or nicotine
  • Current or history of severe alcohol withdrawal
  • MRI/tACS contraindications including pregnancy
  • Impaired hearing (psychotherapy using American Sign Language is not possible)
  • Insufficient corrected visual acuity to complete assessments
  • Unable to read or speak English fluently
  • Unable to provide valid informed consent

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Motivational Interviewing with Brain Stimulation or Sham

Duration - 1 session

Participants receive a motivational interviewing session lasting about 30 minutes combined with either active transcranial alternating current stimulation (tACS), sham stimulation, or no stimulation for the delayed treatment control group.

1 visit (in-person)

Brain Imaging Assessment

Duration - 1 to 2 visits depending on group assignment

Participants in the tACS and sham stimulation groups undergo magnetoencephalography (MEG) and MRI scans to measure brain activity and structure.

1 to 2 visits (in-person)

Follow-up Assessment

Duration - 1 month after intervention

One month after the intervention session, participants complete an online assessment reporting their alcohol use during the prior 30 days.

1 online visit

Trial Site Locations

Total: 1 location

1

The Mind Research Network

Albuquerque, New Mexico, United States, 87106

Actively Recruiting

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Research Team

J

Jon M Houck, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

3

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