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An investigation on the repetitive transcranial focused ultrasound stimulation on the neural mechasim on the cognitive functions in patients of obseesive-compulsive disorder, major depressive disorder and addiction disorder

An investigation on the repetitive transcranial focused ultrasound stimulation on the neural mechasim on the cognitive functions in patients of obseesive-compulsive disorder, major depressive disorder and addiction disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074893
Enrollment
Unknown
Registered
2023-08-18
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

OCD, MDD, Addction

Interventions

theta-burst TUS:The NeuroFUS Pro transcranial ultrasound stimulator is used, consisting of the Transducer Power Output TPO-203 and a four-element transducer CTX-500. The ultrasound stimulation paramet
40-s offline protocol:The NeuroFUS Pro transcranial ultrasound stimulator (using Transducer Power Output TPO-203 and a four-element transducer CTX-500) is employed. The ultrasound stimulation paramete

Sponsors

Zhongshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
22 Years to 50 Years

Inclusion criteria

Inclusion criteria: Healthy Controls: 1) Age 18-60 years, both males and females, right-handed. 2) No clear diagnosis of physical or mental illness. 3) Signed informed consent form. 4) Normal vision or corrected visual acuity. 5) Participants capable of completing the specified tests according to the protocol. Psychiatric Patients: 1) Age 18-60 years, both males and females, right-handed. 2) Primary diagnosis of one of the following mental disorders (meeting DSM-V diagnostic criteria): obsessive-compulsive disorder, depression, substance addiction (including but not limited to nicotine, alcohol, heroin, methamphetamine, or methadone). 3) Disease severity: For obsessive-compulsive disorder patients, Yale-Brown Obsessive-Compulsive Scale score > 19; for depression patients, Hamilton Depression Rating Scale 17-item total score = 17; for substance addiction patients, at least 3 previous failed attempts at abstinence. 4) Stable medication treatment plan in the past month. 5) Signed informed consent form. 6) Normal vision or corrected visual acuity. 7) Participants capable of completing the specified tests according to the protocol.

Exclusion criteria

Exclusion criteria: 1. Applicable to all participants: a) Abnormal cognitive status (assessed using MoCA with a score 19. 3. Psychiatric Patients: a) Previous or concurrent neurological disorders: cerebrovascular disease, central nervous system infections, Creutzfeldt-Jakob disease, Huntington's disease, Parkinson's disease, frontotemporal dementia, traumatic brain injury-related dementia, other physical and chemical factors (drugs, alcohol, CO, etc.), significant physical diseases (hepatic encephalopathy, pulmonary encephalopathy, etc.), intracranial space-occupying lesions (subdural hematoma, brain tumors), endocrine system disorders (thyroid disease, parathyroid disease), and any dementia caused by vitamin or other reasons. b) Comorbidities with other psychiatric disorders (e.g., comorbid depression in patients with obsessive-compulsive disorder).

Design outcomes

Primary

MeasureTime frame
Behavioral outcome;Clinical outcome;Physiological outcome;

Countries

China

Contacts

Public ContactWenjuan Liu

Zhongshan Hospital

liu.wenjuan@zs-hospital.sh.cn+86 137 7436 6515

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026