Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

HD-tDCS during CBT for Cocaine Use Disorder

Official title: Open-label Feasibility Trial of HD-tDCS During Cognitive Behavioral Therapy for Cocaine Use Disorder

Run by Virginia Commonwealth University · NCT07829263 · Data updated 2026-11-12

This study tests whether adding high-definition transcranial direct current stimulation to cognitive behavioral therapy helps adults with cocaine use disorder see if CBT works better.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment36 (estimated)
SponsorVirginia Commonwealth University
Academic / other
Locations1 site (Richmond, Virginia)
StatusRecruiting
StartedOctober 2026
Main results expectedDecember 2027
Study endsDecember 2027
Registry record updatedSeptember 28, 2026
Trial IDNCT07829263 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18-65 with DSM-5 cocaine use disorder (moderate to severe) who show interest in treatment and have a positive cocaine metabolite urine test at screening.

Probably not a fit

Individuals with other active substance use disorders (besides mild alcohol or cannabis use disorder), certain medical or neurological conditions, or those on medications that lower seizure threshold may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This open-label feasibility study explores the safety and practicality of using high-definition transcranial direct current stimulation (HD-tDCS) over the dorsolateral prefrontal cortex in combination with cognitive behavioral therapy for adults with moderate to severe cocaine use disorder. The goal is to determine whether this neurobiological approach can support CBT by improving cognitive function and treatment engagement. Participants receive HD-tDCS while undergoing standard CBT, under monitored conditions, to assess tolerability, adherence, and potential signals of benefit. The trial will inform future larger studies on whether this combined approach can reduce cocaine use and enhance cognitive performance in this population. Enrollment is limited to adults aged 18-65 meeting DSM-5 criteria for cocain e use disorder with a positive urine screen at screening.

Why it matters

Potential benefit: If successful, participants may experience improved cognitive functioning and greater engagement with CBT, potentially reducing cocaine use.

How similar studies have gone: HD-tDCS over DLPFC has shown cognitive benefits in other contexts, but its use to augment CBT for cocaine use disorder is exploratory and not yet established in large trials.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria

* Between 18 and 65 years-of-age.
* Meet current DSM-5 criteria for Cocaine Use Disorder (CocUD), moderate or severe
* Professed interest in CocUD treatment or reducing cocaine use.
* Understand and comply with study procedures
* Positive urine result for cocaine metabolite in at least one screening visit.

Exclusion Criteria

* Current DSM-5 diagnosis of any non-cocaine substance use disorder (SUD) other than alcohol use disorder-mild or cannabis use disorder-mild
* Epilepsy or a history of multiple seizures
* Taking any medications known to reduce seizure threshold
* History of migraines, ringing in the ears, and/or a head injury that resulted in a diagnosis of concussion and/or loss of consciousness
* Current scalp condition (e.g. psoriasis) or head wound that has not completely healed
* Currently pregnant or hoping to become pregnant at any point during the study
* Significant current suicidal or homicidal ideation
* Metal plate in skull or other embedded metal fragments in body or other bodily metal
* Claustrophobia or other MRI contraindications
* Fitted with electrical implants such as pacemaker
* Present with clinically significant symptoms of acute cocaine or opioid withdrawal (these individuals would be rescheduled after resolution of acute withdrawal, if possible).

Where it's running

  • Virginia Commonwealth University
    Richmond, Virginia, United States
    Recruiting

Study contacts

  • Principal investigator: James Bjork — Virginia Commonwealth University
  • Study coordinator: Brooke Moorman
  • Email: dneurolab@vcu.edu
  • Phone: 804-828-6494

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.