Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
NCT04871048

Examining tDCS Effect on Cannabis Use Disorder in Patients With Schizophrenia

Led by Centre Hospitalier Universitaire de Saint Etienne · Updated on 2026-05-06

110

Participants Needed

8

Research Sites

384 weeks

Total Duration

On this page

Sponsors

C

Centre Hospitalier Universitaire de Saint Etienne

Lead Sponsor

D

Direction Générale de l'Offre de Soins

Collaborating Sponsor

AI-Summary

What this Trial Is About

Cannabis use disorder is a frequent comorbidity of schizophrenia, associated with increased symptoms and less adherence to therapy. Validated care has limited effectiveness in this population and development of new management strategies seems necessary. Transcranial direct current stimulation (tDCS) has shown beneficial effects in both schizophrenia, substance use disorder and, in a less extent, in nicotine addiction in schizophrenic subjects. It is interesting to test if that 10 sessions of anodal stimulation of the right dorsolateral prefrontal cortex (DLPFC) and cathodal stimulation of the medial prefrontal cortex (MPFC) (by increasing control and modulating reward system), will reduce, in 110 schizophrenic subjects, cannabis consumption, and secondly craving, addiction severity, schizophrenic symptoms and improve global functioning. It is possible that these clinical effects will be associated with changes in certain cognitive functions and cerebral connectivity.

CONDITIONS

Official Title

Examining tDCS Effect on Cannabis Use Disorder in Patients With Schizophrenia

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of schizophrenia according to DSM 5 criteria with stable psychotropic treatment for at least 4 weeks
  • Moderate to severe cannabis use disorder according to DSM 5 with active cannabis use in the last 7 days
  • Motivation to reduce or quit cannabis consumption
  • Patients under ambulatory compulsory care may participate
Not Eligible

You will not qualify if you...

  • Presence of other substance use disorders except nicotine according to DSM 5
  • Any other current psychiatric disorder except personality disorder according to DSM 5
  • Currently hospitalized as an inpatient
  • History of head injury, neurological disorder with brain impact, or severe unstable physical illness
  • Pregnancy or absence of contraception
  • Contraindications to tDCS or MRI such as implanted devices, uncontrolled epilepsy, or intracranial hypertension

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 8 locations

1

CH Le Vinatier Service universitaire d'addictologie de Lyon

Bron, France, 69678

Not Yet Recruiting

2

Centre Hospitalier Universitaire Service d'Addictologie et Pathologies Duelles

Clermont-Ferrand, France, 63000

Not Yet Recruiting

3

CHU de Clermont-Ferrand Service de Psychiatrie

Clermont-Ferrand, France, 63000

Not Yet Recruiting

4

Service Hospitalo-Universitaire d'Addictologie CHU de Dijon

Dijon, France, 21079

Not Yet Recruiting

5

CHU Pôle de Psychiatrie Neurologie et Rééducation

La Tronche, France, 38700

Not Yet Recruiting

6

CH Saint-Cyr-au-Mont-d'Or service de psychiatrie

Saint-Cyr-au-Mont-d'Or, France, 69450

Not Yet Recruiting

7

Centre Hospitalier Alpes Isère

Saint-Égrève, France, 38120

Not Yet Recruiting

8

CHU de Saint-Etienne

Saint-Priest-en-Jarez, France

Actively Recruiting

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Research Team

A

Aurelia GAY, MD

CONTACT

B

Béatrice DEYGAS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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