Tdcs And cogNitive traininG cOmbined for AUD (TANGO)
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Alcohol Use Disorder, Addiction
In brief
The overarching goal of this project is to expand the traditional expertise in non-invasive neuromodulation at the University of Minnesota towards developing novel paired-neuromodulation approaches using transcranial direct current stimulation (tDCS) for new treatments for alcohol use disorder (AUD) that support long-term abstinence. This study will allow the investigators to discern whether the pairing of dorsolateral prefrontal cortex (DLPFC) stimulation and cognitive training can lead to improved treatment outcomes as it pertains to executive functioning and maintenance of abstinence. This paired-neuromodulation approach can potentially be used as a therapeutic intervention to decrease relapse probability in addiction. The long-term goal is to develop new addiction treatments that support long-term abstinence. The exploratory goal of this research is to associate genotypes and epigenetic changes with variations in intervention response and clinical outcome. Individual differences in baseline genetic profiles or epigenetic changes over the course of treatment could be associated with treatment response variability.
Key facts
- Study ID
- NCT05062369
- Run by
- University of Minnesota
- People needed
- 40
- Starts
- 2022-03-03
- Expected to finish
- 2027-09-30
- Last updated by the study team
- 2025-10-09
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Meet the Diagnostic and Statistical Manual of Mental Disorders diagnostic criteria for AUD
- Abstinent from alcohol use
- Must have the intention to remain in the Lodging Plus program until the end of the intervention portion of the study.
You may not qualify if…
- Any medical condition or treatment with neurological sequelae (i.e. stroke, tumor, loss of consciousness>30 min, HIV)
- A head injury resulting in a skull fracture or a loss of consciousness exceeding 30 minutes (i.e., moderate or severe TBI)
- Any contraindications for tDCS or MRI scanning (tDCS contraindication: history of seizures; MRI contraindications; metal implants, pacemakers or any other implanted electrical device, injury with metal, braces, dental implants, non-removable body piercings, pregnancy, breathing or moving disorder)
- Any primary psychotic disorder (e.g. schizophrenia, schizoaffective disorder); Participants with other treated and stable psychiatric disorders will be included
- Presence of a condition that would render study measures difficult or impossible to administer or interpret
- Primary current substance use disorder diagnosis on a substance other than alcohol except for caffeine or nicotine
- Clinical evidence for Wernicke-Korsakoff syndrome
- Left-handedness
- Entrance to the treatment program under a court mandate
Where it is running
- University of Minnesota — Minneapolis, Minnesota, United States (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.