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Noninvasive Brain Stimulation
Transcranial Electrical Stimulation for Hallucinations
N/A
Recruiting
Led By Paulo Lizano, MD, PhD
Research Sponsored by Beth Israel Deaconess Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Actively experiencing hallucinations (tactile, auditory, visual, etc.)
Aged 18-50 years of age
Must not have
History of seizures
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline to month follow-up
Summary
This trial uses a technique that applies a weak electrical current to the scalp to help patients with psychotic disorders who experience hallucinations. The treatment targets a specific brain area involved in processing sensory information to reduce abnormal activity and alleviate hallucinations. This non-invasive brain stimulation technique enhances the precision of the treatment by using smaller electrodes.
Who is the study for?
This trial is for English-speaking adults aged 18-50 who are currently experiencing hallucinations. It's not suitable for those with recent substance abuse, pregnant or breastfeeding individuals, people with significant head injuries, intellectual disabilities, metal implants in the body (especially in the head), or a history of seizures.
What is being tested?
The study tests Transcranial Electrical Stimulation (tES) targeted at the right superior temporal sulcus (rSTS) to see if it can improve brain activity and reduce hallucinations in psychotic disorders like schizophrenia.
What are the potential side effects?
Potential side effects of tES may include discomfort at the stimulation site, headache, dizziness, nausea or itching under the electrodes during application. There's also a low risk of inducing seizures.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am currently experiencing hallucinations.
Select...
I am between 18 and 50 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have a history of seizures.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline to month follow-up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline to month follow-up
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
7-item Auditory Hallucinations Rating Scale (AHRS)
Positive and Negative Syndrome Scale (PANSS)
University of Miami Parkinson's Disease Hallucinations Questionnaire (UM-PDHQ)
Secondary study objectives
Auditory Steady state evoked potential
Biological motion
Brief Assessment of Cognition (BACS)
+8 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Active Stimulation with TDCSExperimental Treatment1 Intervention
10 tDCS; Two, twenty-minute sessions of tDCS to the rSTS for 5 days (10 total sessions).
Group II: SHAM StimulationPlacebo Group1 Intervention
10 passive sham control; Two, twenty-minute sessions of passive sham control to the rSTS for a 30 second ramped up and down at the beginning and end of the 20 min period for 5 days (10 total sessions).
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Transcranial Electrical Stimulation
2019
Completed Early Phase 1
~20
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
Noninvasive brain stimulation techniques like transcranial magnetic stimulation (TMS) and transcranial direct current stimulation (tDCS) are commonly used to treat auditory hallucinations. TMS uses magnetic fields to stimulate nerve cells in specific brain regions, such as the dorsolateral prefrontal cortex, which can help modulate abnormal brain activity associated with hallucinations. tDCS, on the other hand, uses a low electrical current to alter neuronal activity and improve connectivity in targeted areas of the brain.
These treatments matter for patients with auditory hallucinations because they offer a noninvasive way to potentially reduce the frequency and severity of hallucinations by directly influencing brain function and sensory processing.
Find a Location
Who is running the clinical trial?
Beth Israel Deaconess Medical CenterLead Sponsor
853 Previous Clinical Trials
12,930,901 Total Patients Enrolled
4 Trials studying Psychosis
249 Patients Enrolled for Psychosis
Paulo Lizano, MD, PhDPrincipal InvestigatorBeth Israel Deaconess Medical Center
1 Previous Clinical Trials
1 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am currently experiencing hallucinations.You have an intellectual disability according to the DSM-V guidelines.I am between 18 and 50 years old.I have a history of seizures.You have metal in your body that cannot be taken out, especially near your head.You have a history of head injury with more than 15 minutes of unconsciousness or lasting problems from the injury.You have struggled with substance abuse or addiction in the last 6 months.You have not received tES/TMS treatments recently.
Research Study Groups:
This trial has the following groups:- Group 1: SHAM Stimulation
- Group 2: Active Stimulation with TDCS
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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