Mechanistic Clinical Trial of Individualized tDCS for Hallucinations in Schizophrenia

NCT ID: NCT04248010

Last Updated: 2022-04-05

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-12-31
• Study Completion Date: 2025-06-01

Brief Summary

This project compares standard tDCS to individualized high-definition tDCS (HD-tDCS) for treatment of auditory verbal hallucinations in schizophrenia.

Detailed Description

The large majority of patients with schizophrenia (Sz) experience auditory verbal hallucinations (AVH) as a core feature of their disorder. Treatment-resistant auditory verbal hallucinations (AVH) affect a third of patients with schizophrenia and can cause increased aggression, distress, suicide, and social dysfunction. This project will investigate the efficacy of different types of transcranial direct current stimulation (tDCS), a neurostimulation technique that passes a weak electric current through the brain, in alleviating AVH in Sz patients, and will explore hypotheses regarding brain circuits involved in AVH.

This project compares standard tDCS to individualized high-definition tDCS (HD-tDCS) for treatment of AVH. In standard tDCS, two large electrodes are positioned on the scalp above regions of the brain implicated in abnormal cortical activity associated with auditory verbal hallucinations in Sz. Due to the size of standard tDCS electrodes and the positions required to stimulate language areas, large unrelated areas of the brain are also stimulated. HD-tDCS is a novel technique that uses multiple smaller electrodes to produce a more focal electrical field (EF) than standard tDCS. The HD-tDCS used in this study modulates brain activity in a targeted area without stimulating as many unrelated areas. This targeted inhibition allows us to test hypotheses regarding different cortical regions and their roles in specific features of AVH (e.g. loudness and salience).

Participants are randomized to receive either active standard tDCS or active HD-tDCS targeting one of two language-processing areas of the brain, or a sham version of one of these stimulation types. For each participant receiving HD-tDCS, structural MRI is used to computationally model the electrical field produced in their individual brain anatomy by tDCS. These models are then used to select individualized electrode configurations and current settings to target the same language areas across subjects. The effect of stimulation on relevant brain functions is verified by measuring pre/post treatment changes in resting state functional connectivity (rsFC) within and between targeted language regions, which has been previously linked to AVH symptoms. Differences in behavioral task performance and neurophysiological abnormalities associated with AVH are also tested pre/post treatment.

Conditions

Schizophrenia and Related Disorders

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

standard tDCS

20 min of standard 2-electrode transcranial direct current stimulation (2 mA) at a previously reported scalp location.

Group Type: ACTIVE_COMPARATOR

neuroConn DC-Stimulator MR

Intervention Type: DEVICE

standard tDCS, active \& sham

HD-tDCS - anterior target

20 min of individualized high-density 5-electrode transcranial direct current stimulation to anterior language areas of the brain.

Group Type: ACTIVE_COMPARATOR

Soterix MxN HD-tES

Intervention Type: DEVICE

HD-tDCS, active \& sham

HD-tDCS - posterior target

20 min of individualized high-density 5-electrode transcranial direct current stimulation to posterior language areas of the brain.

Group Type: ACTIVE_COMPARATOR

Soterix MxN HD-tES

Intervention Type: DEVICE

HD-tDCS, active \& sham

sham tDCS

sham transcranial direct current stimulation using a brief pulse at the beginning and end of the 20 min intervention.

Group Type: SHAM_COMPARATOR

neuroConn DC-Stimulator MR

Intervention Type: DEVICE

standard tDCS, active \& sham

Soterix MxN HD-tES

Intervention Type: DEVICE

HD-tDCS, active \& sham

Interventions

neuroConn DC-Stimulator MR

standard tDCS, active \& sham

Intervention Type: DEVICE

Soterix MxN HD-tES

HD-tDCS, active \& sham

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• DSM-V diagnosis of schizophrenia or schizoaffective disorder
• Capacity and willingness to provide informed consent
• Mean AHRS item score of greater or equal to 2.
• If female and not infertile, must agree to use one of the following forms of contraception for the duration of study participation: systemic hormonal treatment, an IUD which was implanted at least 2 months prior to screening, or "double-barrier" contraception. Women of child bearing potential must have a negative pregnancy test at screening
• Right handed
• Normal hearing
• Taking an antipsychotic medication at a stable dose for at least 4 weeks. All oral and depot antipsychotics are allowable.

Exclusion Criteria

• Presence or positive history of unstable significant medical or neurological illness
• Substance use disorder (excluding nicotine) within last 90 days, or positive toxicology screen for any substance of abuse
• Pregnancy
• Participation in study of investigational medication/device within 4 weeks
• History of seizure, epilepsy in self or first-degree relatives, stroke, brain surgery, head injury with loss of consciousness >1 hour or clear cognitive sequelae, intracranial metal implants, known structural brain lesion, devices that may be affected by tDCS (pacemaker, medication pump, cochlear implant, implanted brain stimulator)
• Subjects with suicidal ideation with intent or plan (indicated by affirmative answers to items 4 or 5 of the Suicidal Ideation section of the baseline C-SSRS) in the 6 months prior to screening or subjects who represent a significant risk of suicide in the opinion of the investigator
• Frequent and persistent migraines
• Clinically significant skin disease
• Current use of medications known to lower seizure threshold (Lithium, Theophyline, Tricyclic antidepressants, Buproprion >450 mg/day and Clozapine >600 mg/day, brand name and generic methylphenidate/mixed amphetamine salts)
• History of prior clinically significant, adverse response to neurostimulation or open skin wounds that would preclude safe placement of tDCS electrodes
• Contraindication to MRI scanning, including metal implants or claustrophobia. Metal implants, pacemaker, other metal (e.g., shrapnel or surgical prostheses) or paramagnetic objects contained within the body which may present a risk to the subject or interfere with MR scan
• Medicinal patch, unless removed

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Columbia University

OTHER

Sponsor Role: lead

Responsible Party

Michael Avissar

Assistant Professor of Psychiatry

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

7882

Identifier Type: -

Identifier Source: org_study_id