Actively Recruiting
Combined tDCS and Cognitive Training as an Adjunctive Treatment in Opioid Use Disorder
Led by University of Minnesota · Updated on 2026-02-12
160
Participants Needed
1
Research Sites
25 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The overall goal of this study is to investigate the added benefit of a neuromodulation intervention in individuals under buprenorphine maintenance treatment for OUD (bOUD).
CONDITIONS
Official Title
Combined tDCS and Cognitive Training as an Adjunctive Treatment in Opioid Use Disorder
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Ability to provide consent and follow study procedures
- Diagnosis of opioid use disorder by DSM criteria
- Currently receiving buprenorphine maintenance treatment
- Intend to stay in addiction treatment program until intervention is completed
You will not qualify if you...
- Any medical condition causing neurological problems
- Head injury with skull fracture or loss of consciousness longer than 30 minutes
- Contraindications to tDCS or MRI, including seizures, metallic implants or devices, scalp eczema, pacemakers, shrapnel, metallic braces, non-removable piercings, breathing or movement disorders, claustrophobia, or pregnancy
- Any psychotic disorder (other treated stable psychiatric disorders allowed)
- Condition preventing study measures from being done or interpreted
- Under 18 years old
- Primary current substance use disorder other than opioids except caffeine or nicotine
- Court mandated treatment
- Pregnancy
- Disrespectful behavior toward investigators and staff
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Minnesota
Minneapolis, Minnesota, United States, 55455
Actively Recruiting
Research Team
C
Clarista Berg
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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