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Precise Intervention Technology and Application of Low Intensity TUS on Negative Symptoms of Schizophrenia

Primary Purpose

Negative Symptoms of Schizophrenia

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
low-intensity transcranial ultrasound stimulation (TUS)
Sponsored by
Shanghai Mental Health Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Negative Symptoms of Schizophrenia focused on measuring Schizophrenia, Negative Symptoms, Transcranial Ultrasound Stimulation

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Meet the DSM-5 diagnostic criteria for schizophrenia or schizoaffective disorder; Age18-50, right-handed, Han nationality; Score of at least 1 item from N1 to N7 in PANSS is ≥4 (moderate or above); Be in a stable condition, received second-generation antipsychotics for at least 4 weeks or more; Written informed consent; Exclusion Criteria: Current or past neurological illness, severe physical diseases, substance abuse or alcohol dependence, mental retardation, pregnant or lactation; Uncooperative or risky patients with high excitement, stupor, disorder of words and deeds, negative suicide, etc.; History of MECT or other physical therapy within 6 months; History of epilepsy, or epileptic waves on the baseline EEG; Ruled out share antiepileptic drugs, carbamazepine, valproic acid salt) or larger doses of benzodiazepines drugs (> 10 mg/day, diazepam clonazepam 2 mg/day, 1 mg/day, alprazolam lorazepam 2 mg/day, midazolam 10 mg/day, 20 mg/day, Mr Shah diazepam triazolam 0.5 mg/day), avoid the use of chlorine drug, (in principle, to avoid the use of antiepileptic drugs and clonazepam;Other antipsychotic drugs, if necessary, remain unchanged during the course of treatment; Contraindications to TUS and MRI are present.

Sites / Locations

  • Shanghai Mental Health Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Sham Comparator

Arm Label

single-target group (left DLPFC)

both-target group (both left DLPFC and right STG)

sham group

Arm Description

34 eligible patients will be treated with active TUS for 4 weeks on the left DLPFC

34 eligible patients will be treated with active TUS for 4 weeks on the both left DLPFC and right STG

34 eligible patients will be treated with sham TUS for 4 weeks on the left DLPFC

Outcomes

Primary Outcome Measures

Change from baseline in the Scale for Assessment of Negative Symptoms(SANS)
Change from baseline in the Scale for Assessment of Negative Symptoms(SANS) at 4 weeks and 8 weeks. The minimum to maximum value is 0-120. Lower scores mean a better outcome.
Change from baseline in Positive and Negative Syndrome Scale(PANSS)
Change from baseline in Positive and Negative Syndrome Scale(PANSS) at 4 weeks and 8 weeks. The minimum to maximum value is 30-210. Lower scores mean a better outcome.

Secondary Outcome Measures

Cognitive Function
Change from baseline in MATRICS MCCB
Change of Multi-modal Brain Neuroimaging in structure
Brain structure data will be acquired.
Change of Multi-modal Brain Neuroimaging in resting- state fMRI
Resting-state fMRI data will be acquired.
Change of Multi-modal Brain Neuroimaging in 1H-MRS
1H-MRS data will be acquired.
Change of functional near-infrared spectroscopy (fNIRS)
Functional near-infrared spectroscopy (fNIRS), a non-invasive neuroimaging technique that reflects changes in Oxy-Hb and Deoxy-Hb during brain activity, will be measured on left M1 region at baseline to evaluate the neuromodulation effect of TUS on neural activity.

Full Information

First Posted
July 17, 2023
Last Updated
August 10, 2023
Sponsor
Shanghai Mental Health Center
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1. Study Identification

Unique Protocol Identification Number
NCT05985993
Brief Title
Precise Intervention Technology and Application of Low Intensity TUS on Negative Symptoms of Schizophrenia
Official Title
Precise Intervention Technology and Application of Low Intensity Transcranial Ultrasound Stimulation (TUS) on Negative Symptoms of Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 1, 2023 (Anticipated)
Primary Completion Date
July 31, 2025 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Mental Health Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Based on the current background and our previous studies, TUS has been proved that rTUS intervention could induce long-term potentiation like (LTP-like) plasticity and neuromodulate the brain cortex in schizophrenia patients. rTUS over the left dorsolateral prefrontal cortex (DLPFC) can alleviate the negative symptoms in schizophrenia. In this double-blind, randomized, sham-controlled study, the efficacy of different treatment options and mechanisms of low-intensity rTUS on negative symptoms will be investigated.
Detailed Description
Negative symptoms is a core symptom of schizophrenia related to poor functional outcome which remains largely treatment refractory. Prior studies indicated that abnormalities in the prefrontal-temporal circuit and glutamate/GABA imbalances may be the root causes of negative symptoms. Transcranial ultrasound stimulation (TUS), an emerging non-invasive neuromodulation technique, can modulate neural excitability and plasticity in the prefrontal and temporal cortex. In this double-blind, randomized, sham-controlled study, the efficacy of different treatment options and mechanisms of low-intensity rTUS on negative symptoms will be investigated. A total of 102 schizophrenia inpatients will be recruited and randomly allocated into single-target group (left DLPFC), both-target group (both left DLPFC and right STG) or sham group in ratio of 1:1:1. This study aims to determine the efficacy of TUS and to reveal its underlying neural mechanism. MEPs, fNIRS ,and multi-modal MRI will be detected. Neuropsychological assessments will also be conducted to develop the optimized treatment strategy. The study points to a novel and promising therapeutic neuromodulation approach that may improve the functional outcome of schizophrenia, which has been the main cause of mental disability.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Negative Symptoms of Schizophrenia
Keywords
Schizophrenia, Negative Symptoms, Transcranial Ultrasound Stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
102 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
single-target group (left DLPFC)
Arm Type
Active Comparator
Arm Description
34 eligible patients will be treated with active TUS for 4 weeks on the left DLPFC
Arm Title
both-target group (both left DLPFC and right STG)
Arm Type
Active Comparator
Arm Description
34 eligible patients will be treated with active TUS for 4 weeks on the both left DLPFC and right STG
Arm Title
sham group
Arm Type
Sham Comparator
Arm Description
34 eligible patients will be treated with sham TUS for 4 weeks on the left DLPFC
Intervention Type
Device
Intervention Name(s)
low-intensity transcranial ultrasound stimulation (TUS)
Intervention Description
The rTUS was administered using an immersion-type focused ultrasound transducer (V391-SU, Olympus NDT, Waltham, USA). Low-intensity transcranial ultrasound stimulation on the target. Duration:20 days (workdays for four consecutive weeks).
Primary Outcome Measure Information:
Title
Change from baseline in the Scale for Assessment of Negative Symptoms(SANS)
Description
Change from baseline in the Scale for Assessment of Negative Symptoms(SANS) at 4 weeks and 8 weeks. The minimum to maximum value is 0-120. Lower scores mean a better outcome.
Time Frame
baseline, 4 weeks and 8 weeks
Title
Change from baseline in Positive and Negative Syndrome Scale(PANSS)
Description
Change from baseline in Positive and Negative Syndrome Scale(PANSS) at 4 weeks and 8 weeks. The minimum to maximum value is 30-210. Lower scores mean a better outcome.
Time Frame
baseline, 4 weeks and 8 weeks
Secondary Outcome Measure Information:
Title
Cognitive Function
Description
Change from baseline in MATRICS MCCB
Time Frame
baseline, 4 weeks and 8 weeks
Title
Change of Multi-modal Brain Neuroimaging in structure
Description
Brain structure data will be acquired.
Time Frame
baseline and 4 weeks
Title
Change of Multi-modal Brain Neuroimaging in resting- state fMRI
Description
Resting-state fMRI data will be acquired.
Time Frame
baseline and 4 weeks
Title
Change of Multi-modal Brain Neuroimaging in 1H-MRS
Description
1H-MRS data will be acquired.
Time Frame
baseline and 4 weeks
Title
Change of functional near-infrared spectroscopy (fNIRS)
Description
Functional near-infrared spectroscopy (fNIRS), a non-invasive neuroimaging technique that reflects changes in Oxy-Hb and Deoxy-Hb during brain activity, will be measured on left M1 region at baseline to evaluate the neuromodulation effect of TUS on neural activity.
Time Frame
baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meet the DSM-5 diagnostic criteria for schizophrenia or schizoaffective disorder; Age18-50, right-handed, Han nationality; Score of at least 1 item from N1 to N7 in PANSS is ≥4 (moderate or above); Be in a stable condition, received second-generation antipsychotics for at least 4 weeks or more; Written informed consent; Exclusion Criteria: Current or past neurological illness, severe physical diseases, substance abuse or alcohol dependence, mental retardation, pregnant or lactation; Uncooperative or risky patients with high excitement, stupor, disorder of words and deeds, negative suicide, etc.; History of MECT or other physical therapy within 6 months; History of epilepsy, or epileptic waves on the baseline EEG; Ruled out share antiepileptic drugs, carbamazepine, valproic acid salt) or larger doses of benzodiazepines drugs (> 10 mg/day, diazepam clonazepam 2 mg/day, 1 mg/day, alprazolam lorazepam 2 mg/day, midazolam 10 mg/day, 20 mg/day, Mr Shah diazepam triazolam 0.5 mg/day), avoid the use of chlorine drug, (in principle, to avoid the use of antiepileptic drugs and clonazepam;Other antipsychotic drugs, if necessary, remain unchanged during the course of treatment; Contraindications to TUS and MRI are present.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dengtang LIU
Phone
021-34773434
Email
erliu110@126.com
Facility Information:
Facility Name
Shanghai Mental Health Center
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200030
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dengtang LIU
Phone
021-34773434
Email
erliu110@126.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Precise Intervention Technology and Application of Low Intensity TUS on Negative Symptoms of Schizophrenia

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