tACS-MI: A Pilot Study of Non-invasive Brain Stimulation to Boost the Efficacy of Psychotherapy in a Community Sample of People Who Drink Alcohol
Study Details
Study Description
Brief Summary
The goal of this small (n=75) proof-of-concept randomized clinical trial is to test the effects of transcranial alternating current stimulation (tACS) during motivational interviewing (MI) sessions with participants who drink at above the low-risk level. Participants will be randomized to receive either MI with active stimulation, MI with sham stimulation, or a delayed treatment group that receives MI with no stimulation. Measures will include brain imaging, alcohol use, cannabis use, risk-taking behavior, emotions, and others. Participants who are randomized to the delayed-treatment group will not receive brain imaging.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
This proof-of-concept randomized clinical trial will recruit n=75 people with problematic levels of drinking who are considering treatment for their alcohol use. These participants will be randomized to one of three conditions: a condition that applies active tACS during an MI session (MI+tACS), a condition that applies sham stimulation during an MI session (MI+sham), or a waitlist control condition (MI-only). Only participants the MI+tACS and MI+sham conditions will be included in the brain imaging portion of the study. One month after their intervention session, all participants will report their use of alcohol in the prior 30 days via an online assessment battery. This will allow us to test the effects of tACS on within-session client speech and outcomes.
Participants will have magnetoencephalography (MEG) scans including rest and an alcohol cue task to measure the acute effects of brain stimulation. Participants will also have MRI scans including structure and rest. The Motivational Interviewing Skill Code (MISC 2.5) and the CASAA Application for Coding Treatment Interactions (CACTI) will be used to assess counselor and participant speech in the recorded MI sessions and to ensure that sessions comply with the principles of MI.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: MI with tACS Motivational interviewing with concurrent active stimulation |
Device: High-density transcranial alternating current stimulation
High-density electrode configuration with transcranial alternating current stimulation in the beta (15-40Hz) frequency range
Behavioral: Motivational interviewing
Motivational interviewing session focused on alcohol use, approximately 30 minutes in length
|
| Sham Comparator: MI with sham Motivational interviewing with concurrent sham stimulation |
Device: Sham stimulation
High-density electrode configuration with sham stimulation
Behavioral: Motivational interviewing
Motivational interviewing session focused on alcohol use, approximately 30 minutes in length
|
| Active Comparator: MI-only Motivational interviewing only, delayed treatment control |
Behavioral: Motivational interviewing
Motivational interviewing session focused on alcohol use, approximately 30 minutes in length
|
Outcome Measures
Primary Outcome Measures
- Heavy drinking days [One month]
Number of heavy drinking days in the prior 30 days
Secondary Outcome Measures
- Drinks per drinking day [One month]
Number of drinks per drink day in the prior 30 days
- Percent days abstinent [One month]
Percent days abstinent in the prior 30 days
Eligibility Criteria
Criteria
Inclusion criteria:
-
Self-identify as having problem drinking
-
Right-handed
-
Age 21-60 years
-
AUDIT score indicating risky drinking
Exclusion criteria:
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Left-handed or ambidextrous
-
Currently engaged in treatment for alcohol use disorder
-
Receiving treatment for alcohol use disorder within the prior 12 months
-
History of brain injury or neurological diagnosis
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Evidence of current psychosis
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Past-year substance use disorder other than alcohol, marijuana, or nicotine
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Current or history of severe alcohol withdrawal
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MRI/tACS contraindications including pregnancy
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Impaired hearing (psychotherapy using American Sign Language is not possible within the scope of the proposed study)
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Insufficient corrected visual acuity to complete the assessment instruments
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Unable to read/speak English fluently
-
Unable to provide valid informed consent
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The Mind Research Network | Albuquerque | New Mexico | United States | 87106 |
Sponsors and Collaborators
- The Mind Research Network
- National Institute of General Medical Sciences (NIGMS)
Investigators
None specified.Study Documents (Full-Text)
More Information
Publications
None provided.- 20-010
- P30GM122734