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Characteristic analysis of brain function in traumatic brain injury patients with cognitive impairment based on near-infrared imaging of brain function

Characteristic analysis of brain function in traumatic brain injury patients with cognitive impairment based on near-infrared imaging of brain function

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052689
Enrollment
Unknown
Registered
2021-11-03
Start date
2021-11-01
Completion date
Unknown
Last updated
2022-08-08

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

Conditions

traumatic brain injury patients with cognitive impairmen

Interventions

grouptraumatic brain injury group:No
healthy control group:No

Sponsors

The Second Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Hospitalized patients with traumatic brain injury; 2. Course of disease >= 1 month and <= 12 months; 3. Stable condition and stable vital signs; 4. Aged 18 to 85 years; 5. Not taking or injecting drugs that affect cognitive function within 1 month before enrollment; 6. Specialist assessment suggests cognitive impairment; 7. Voluntary participation, informed consent signed by the patient himself or his immediate family.

Exclusion criteria

Exclusion criteria: 1. Unconscious and difficult to complete the experiment; 2. Combined with severe neurological diseases; 3. People with severe mental illness or other mental disorders; 4. Cognitive impairment caused by other types of diseases, such as stroke, dementia with Lewy bodies, Pick disease, AD and other cognitive impairment; 5. The investigator believes that there is any situation that may harm the subject or cause the subject to be unable to meet or perform the research requirements; 6. Those with severe vision and hearing impairments; 7. Intracranial implantation of metal and electronic equipment; after skull defect and metal skull repair; 8. Disabled for patients with implanted electronic devices (such as pacemaker carriers); 9. Participating in another clinical trial.

Design outcomes

Primary

MeasureTime frame
Resting brain function connection;Verbal fluency test, VFT;

Secondary

MeasureTime frame
Changes in Montreal Cognitive Assessment Scale (MOCA) scores;mini-Mental Status examination;clinical dementia rating;Event related potential P300;

Countries

China

Contacts

Public ContactZhang Qiaojun

The Second Affiliated Hospital of Xi'an Jiaotong University

zhangqj@mail.xjtu.cn+86 13891867155

Outcome results

None listed

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