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Research and application of whole-process brain health monitoring and intervention based on multimodal artificial intelligence

Research and application of whole-process brain health monitoring and intervention based on multimodal artificial intelligence

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300067399
Enrollment
Unknown
Registered
2023-01-06
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Parkinson's disease, dementia, anxiety/depression, insomnia disorders

Interventions

Gold Standard:The diagnosis of PD is based on the clinical diagnostic criteria for Parkinson's disease introduced by the International Movement Disorder Society (MDS) in 2015
AD is based on the Alzheimer's Association (NIA-AA) criteria of the National Institute on Aging in 2011
anxiety disorders and depression disorders The diagnosis was based on the tenth edition of the International Statistical Classification of Diseases and Related Health Problems (ICD-10) criteria
the third edition of the International Classification of Sleep Disorders (ICSD-3) was used for insomnia.
Index test:Magnetic resonance neurite direction dispersion and density imaging, functional near-infrared spectroscopy imaging technology, ear EEG, polysomnography, heart rate variability, virtual real

Sponsors

The Second Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with neurodegenerative diseases such as Parkinson's disease (PD), Alzheimer's disease (AD), anxiety/depression disorder, insomnia disorder and age-matched healthy people hospitalized in the Department of Neurology of the Second Affiliated Hospital of Dalian Medical University were selected.

Exclusion criteria

Exclusion criteria: 1. People with pacemaker implantation; 2. Have a history of brain surgery; 3. There are metal implants or other foreign bodies in the brain; 4. Cochlear implant recipients; 5. Patients with a history of epileptic seizures or a family history of epilepsy; 6. Acute traumatic brain injury, cerebral hemorrhage, cerebral infarction patients; 7. Patients with a history of organic diseases such as intracranial infection; 8. Patients who are pregnant, breastfeeding, or have the possibility or plan of pregnancy; 9. Participating in other clinical trials; 10. Acute vertigo; 11. Severe visual impairment or corrected vision can not see the cursor clearly, color blindness, color weakness, strabismus, amblyopia, congenital nystagmus; 12. Taking central sedative drugs, antiepileptic drugs and other drugs affecting the vestibular system 72 hours before the examination; 13. In the resting state, there is obvious tremor in the head. 14. Cannot perform CT or MRI examination for any reason, or cannot cooperate with clinical assessment, laboratory or imaging assessment follow-up (such as severe dementia or mental disorder, severe metabolic disease, any advanced disease leading to life expectancy < 6 months) wait); 15. The researchers judged that they are not suitable for participating in this experiment.

Design outcomes

Primary

MeasureTime frame
intracellular volume fraction;isotropic volume fraction;Directional Dispersion Index;mean oxyhemoglobin concentration;scanning range;scaning latency;saccadic velocity;

Countries

China

Contacts

Public ContactLin Yongzhong

The Second Hospital of Dalian Medical University

lin19671024@163.com+86 177 0987 3166

Outcome results

None listed

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