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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04389528
Other study ID # 10477M-TCC
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 17, 2018
Est. completion date December 17, 2021

Study information

Verified date May 2020
Source Centre hospitalier de Ville-Evrard, France
Contact Youcef BENCHERIF
Phone 0143093232
Email y.bencherif@epsve.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cannabis is the most frequently consumed drug in France and its use continues to increase. Over the 18-64 age group as a whole, experimentation with cannabis at least once in a lifetime increased from 33% in 2010 to 42% in 2014, confirming the upward trend observed since the 1990.

Cannabis, like all drugs, disrupts the reward circuit whose neurons originate in the ventral tegmental area and project into the mesolimbic and cortical structures.

Acute cannabis use is thought to increase mesolimbic dopamine by affecting the Gabaergic or Glutamatergic system.

Chronic cannabis use usurps the reward system and leads to changes in the mesolimbic circuit (nucleus accumbens, ventral tegmental area, amygdala, and prefrontal cortex), inducing increased craving, with persistent craving for the substance and vulnerability to relapse.

Cognitively, addiction is associated with increased impulsivity, with a propensity to take risks leading to impaired decision-making.

There is currently no validated drug treatment for cannabis addiction. Non-invasive brain stimulation could be an interesting therapeutic alternative.


Recruitment information / eligibility

Status Recruiting
Enrollment 78
Est. completion date December 17, 2021
Est. primary completion date July 17, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 63 Years
Eligibility Inclusion Criteria:

1. Men or women between 18 and 65 years of age

2. Right-Handers

3. Diagnosis: Cannabis Use Disorder (according to DSM 5 criteria)

4. Patient with no other drug or psychotherapeutic treatment for cannabis addiction ("naive" patients)

5. Reported use of cannabis more than three times a week in the past three years

6. Signing consent to participate in research

Exclusion Criteria:

1. Pregnancy or lack of effective contraception

2. Patients with severe somatic disease

3. Other addictions of "moderate" to "severe" intensity according to DSM 5 criteria (excluding tobacco and coffee)

4. Patients undergoing antidepressant or neuroleptic or thyroid-regulating therapy.

5. Contraindications to tDCS (presence of an intracranial metal body, intracranial hypertension)

6. Topic that has already been stimulated by tDCS

7. Patients under reinforced guardianship or curatorship

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Neuromodulation by tDCS
The tDCS is a device for modulating cortical excitability. It consists of passing a low intensity direct electrical current over the scalp via two electrodes: an anode and a cathode soaked in a saline solution. Although there is a short-circuit effect through the scalp, a significant amount of electrical current enters the brain and changes the transmembrane potential.

Locations

Country Name City State
France Youcef BENCHERIF Maisons Alfort Île De France

Sponsors (1)

Lead Sponsor Collaborator
Januel

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluating the change from craving to cannabis. by an analog visual scale .Scores (0 to 10) 3 months
Secondary The change to cannabis craving assessed by the Baseline Marijuana Craving Test at the end of treatment 3 month
Secondary The change in cannabis craving during an incentive to use task evaluated by analog visual scale scores (0 to 10) 3 months
Secondary Montgomery-Åsberg depression rating scale) Scores (0 to 60) 3 months
Secondary evaluation of the change in the number of joints consumed per day 3 months
Secondary evaluation of the change in the number of cigarettes consumed per day 3 months
Secondary assessment of the change in attention and inhibition skills as assessed by the Stroop test before and after a neurofeedback test 3 months
Secondary the Gambling Task's assessment of decreased risk-taking 3 months
Secondary Young Mania Rating Scale Scores (0 to 60) 3 months
Secondary Beck Depression Inventory Scores (0 to 39) 3 months
Secondary Clinical Global Impression Severity of disease (0 to 7) 3 months