Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07158853

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Trial Site Locations

Total: 1 location

1

University of Minnesota

Minneapolis, Minnesota, United States, 55455

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here