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Transcranial Direct Current Stimulation

Telehealth tDCS + Mindfulness for Cannabis Use Disorder

N/A
Waitlist Available
Led By Leigh Charvet, PhD
Research Sponsored by NYU Langone Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
All medications stable for ≥ 1 month prior to enrollment and throughout the trial
Definite MS diagnosis, relapsing remitting (RRMS) subtype
Must not have
Seizure disorder or recent (<5 years) seizure history
Meets DSM-V criteria for current panic disorder, obsessive-compulsive disorder, post-traumatic stress syndrome, bipolar affective disorder, schizophrenia, dissociate disorders, and any other psychotic disorder or organic mental disorder
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 6, month 3

Summary

This trial uses mild electrical brain stimulation to help people with a specific type of multiple sclerosis, cannabis dependency, and high stress. The goal is to reduce their stress levels and need for cannabis by improving their decision-making and emotional control. Non-invasive brain stimulation techniques have shown promise in reducing cravings and consumption in similar conditions.

Who is the study for?
This trial is for adults aged 21-65 with Relapse Remitting Multiple Sclerosis (RRMS), mild to moderate distress, and Cannabis Use Disorder who want to reduce or stop cannabis use. Participants must be stable on medications, fluent in English, able to use mobile devices and have internet access.
What is being tested?
The study tests if brain stimulation (tDCS) can lower distress and cannabis use in RRMS patients with CUD. It involves a real tDCS group versus a sham (fake) treatment group, along with mindfulness practices. There will be 46 participants.
What are the potential side effects?
tDCS may cause discomfort at the stimulation site, itching, tingling, headache or fatigue during or after treatment. Mindfulness practice is generally considered safe but could potentially bring up emotional discomfort.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My medications have been the same for at least a month.
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I have been diagnosed with relapsing-remitting multiple sclerosis.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have had seizures or a seizure disorder in the last 5 years.
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I do not have a current diagnosis of severe mental health conditions like schizophrenia or bipolar disorder.
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I have metal implants in my head or neck.
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I have skin issues near where a medical device would be placed.
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I do not have a major neurological, psychiatric, or other medical condition besides MS.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 6, month 3
This trial's timeline: 3 weeks for screening, Varies for treatment, and week 6, month 3 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Age of Onset of Cannabis Use
Secondary study objectives
Change in Cannabis Withdrawal Scale (CWS) Score
Change in Frequency of Cannabis Use
Change in Kessler Psychological Distress Scale (K10) Score
+3 more

Side effects data

From 2018 Phase 2 trial • 54 Patients • NCT01726673
3%
back pain flair up
3%
Myasthenia Gravis
100%
80%
60%
40%
20%
0%
Study treatment Arm
tDCS + Robotic Arm Therapy
tDCS Sham + Robotic Arm Therapy

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Active tDCS + MindfulnessExperimental Treatment2 Interventions
Group II: Sham tDCS + MindfulnessPlacebo Group2 Interventions

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Multiple Sclerosis (MS) include disease-modifying therapies (DMTs) such as interferons, glatiramer acetate, and oral medications like dimethyl fumarate. These treatments primarily work by modulating the immune system to reduce inflammation and prevent immune cells from attacking the myelin sheath, which is crucial for nerve function. For example, interferons reduce the frequency of inflammatory episodes, while glatiramer acetate mimics myelin protein to divert immune attacks. Dimethyl fumarate activates the Nrf2 pathway, providing neuroprotection and reducing oxidative stress. These mechanisms are vital for MS patients as they help manage symptoms, reduce relapse rates, and slow disease progression. Similarly, Dorsolateral Prefrontal Cortex (DLPFC) Transcranial Direct Current Stimulation (tDCS) aims to modulate neuronal activity in the DLPFC to regulate cognitive and emotional functions, potentially offering a non-pharmacological approach to alleviate distress and cognitive symptoms in MS patients.
Effects of left DLPFC versus right PPC tDCS on multiple sclerosis fatigue.

Find a Location

Who is running the clinical trial?

NYU Langone HealthLead Sponsor
1,407 Previous Clinical Trials
855,718 Total Patients Enrolled
23 Trials studying Multiple Sclerosis
2,272 Patients Enrolled for Multiple Sclerosis
Leigh Charvet, PhDPrincipal InvestigatorNYU Langone Health
4 Previous Clinical Trials
41 Total Patients Enrolled
3 Trials studying Multiple Sclerosis
30 Patients Enrolled for Multiple Sclerosis

Media Library

Transcranial Direct Current Stimulation (tDCS) (Transcranial Direct Current Stimulation) Clinical Trial Eligibility Overview. Trial Name: NCT05005013 — N/A
Multiple Sclerosis Clinical Trial 2023: Transcranial Direct Current Stimulation (tDCS) Highlights & Side Effects. Trial Name: NCT05005013 — N/A
Transcranial Direct Current Stimulation (tDCS) (Transcranial Direct Current Stimulation) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05005013 — N/A
~17 spots leftby Nov 2025