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NCT Number: NCT06904092

Efficacy and Mechanisms of TUS on Cognitive Deficits in Schizophrenia: Based on the Hippocampal-Prefrontal Circuit

Cognitive deficit is a core symptom of schizophrenia related to poorer functional outcome. Prior studies indicated that abnormalities in the hippocampus-prefrontal circuit and glutamate/GABA imbalances may lead to cognitive deficits. Based on the current background and our previous studies, it has been proved that TUS can modulate neural excitability and plasticity in the hippocampus. In this double-blind, randomized study, the efficacy of different treatment options and mechanisms of TUS on cognitive deficits will be investigated.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Cognitive deficit is a core symptom of schizophrenia related to poorer functional outcome which remains largely treatment refractory. Prior studies indicated that abnormalities in the hippocampus-prefrontal circuit and glutamate/GABA imbalances may be the root causes of cognitive deficits. Transcranial ultrasound stimulation (TUS), an emerging non-invasive neuromodulation technique with deep penetration ability, can modulate neural excitability and plasticity in the hippocampus. This is a 4-week double-blind randomized trial of TUS for cognitive deficits in schizophrenia, with either left hippocampus or left dorsolateral prefrontal cortex (DLPFC) or both targeted. This study aims to determine the efficacy of TUS and to reveal its underlying neural mechanism, especially with the hippocampus-prefrontal circuit, by means of TUS, as to assess cortical inhibition and excitability, EEG source imaging, and multi-model MRI. 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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Meet the DSM-5 diagnostic criteria for schizophrenia ;
  • Age18-50, right-handed, Han nationality;
  • Presence of cognitive deficit: defined as d' value <0.5 in associative memory test;
  • 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, pregnancy 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 benzodiazepine drugs (diazepam > 10mg/day, clonazepam > 2mg/day etc.), if necessary, remain unchanged during the course of treatment;
  • Contraindications to TUS and MRI are present.

Treatment and study plan

Transcranial Ultrasound Stimulation

Device

The TUS was administered using Transcranial Ultrasound Stimulator UNS-III (model UNS-III), which has passed the safety test for medical electrical equipment (GB9706.1-2007). Transcranial ultrasound stimulation on the target. Duration:20 days (workdays for four consecutive weeks).

Primary outcomes

  1. Change from baseline in associative memory test score

    Time frame: baseline, 4 weeks and 8 weeks

    Change from baseline in the associative memory test score at 4 weeks and 8 weeks.

Secondary outcomes

  1. Change of information processing speed and attention/vigilance

    Time frame: baseline, 4 weeks and 8 weeks

    Change from baseline in 4 MCCB subtests score at 4 weeks and 8 weeks.

  2. Change of working memory

    Time frame: baseline, 4 weeks and 8 weeks

    Change from baseline in N-back task at 4 weeks and 8 weeks. The outcome measures include accuracy, D-prime value, and reaction time.

  3. Change from baseline in Positive and Negative Syndrome Scale(PANSS)

    Time frame: baseline, 4 weeks and 8 weeks

    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.

  4. Change of CGI score

    Time frame: baseline, 4 weeks and 8 weeks

    Change from baseline in Clinical Global Impression (CGI) at 4 weeks and 8 weeks.

  5. Change of Multi-modal Brain Neuroimaging in structure

    Time frame: baseline and 4 weeks

    Brain structure data will be acquired.

  6. Change of Multi-modal Brain Neuroimaging in resting- state fMRI

    Time frame: baseline and 4 weeks

    Resting-state fMRI data will be acquired.

  7. Change of Multi-modal Brain Neuroimaging in 1H-MRS

    Time frame: baseline and 4 weeks

    1H-MRS data will be acquired.

  8. Change of 64 channels EEG

    Time frame: baseline and 4 weeks

    64 channels EEG data will be acquired.

Study contacts

Contact information is provided by the study sponsor or research team.

Dengtang LIU

CONTACT

[email protected]

021-34773434

Sponsors and collaborators

Lead sponsor

Shanghai Mental Health Center

Other

Registry information

Official study title

Efficacy and Mechanisms of Transcranial Ultrasound Stimulation (TUS) on Cognitive Deficits in Schizophrenia:Based on the Hippocampal-Prefrontal Circuit

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Apr 1, 2025
Registry last updated
Jun 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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