China-NINE Cohort:Neuroimmune Network in Elderly / Neurodegeneration
1 other identifier
observational
260
1 country
2
Brief Summary
This is an observational study aimed at understanding the cognitive, functional, and behavioral characteristics of Chinese patients with cognitive impairment, exploring the underlying mechanisms, and providing evidence for early diagnosis, treatment, and care of cognitive disorders including dementia. Eligible participants will undergo a series of assessments and examinations, including cognitive and memory scale tests, routine blood tests, ApoE genetic testing, cerebrospinal fluid testing, brain MRI, functional MRI, and FDG-PET/AV45-PET scans when necessary. Additional samples such as saliva, nasal secretions, and stool may also be collected. Most evaluations are provided free of charge to support diagnosis and treatment guidance. Participation is voluntary. All personal information and research data will be kept confidential. Potential benefits include access to expert clinical care and free cognitive assessments for disease evaluation. Possible inconveniences include time commitment and temporary discomfort during examinations; medical support will be provided if needed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2026
Typical duration for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 16, 2026
CompletedFirst Submitted
Initial submission to the registry
May 6, 2026
CompletedFirst Posted
Study publicly available on registry
May 14, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2029
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2029
May 14, 2026
May 1, 2026
3 years
May 6, 2026
May 8, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Degree and Type of Cognitive Impairment Assessed by Neuropsychological Scales
Higher scores indicate better cognitive function; lower scores indicate more severe cognitive impairment.
From enrollment to the end of treatment at 3 years
Eligibility Criteria
Participants were recruited from Yantai Yuhuangding Hospital, Yantai, Shandong Province, China.
You may qualify if:
- Participants with clinically diagnosed cognitive impairment. Patients with clinically diagnosed Parkinson's disease. Healthy control participants.
You may not qualify if:
- Central nervous system infection, head trauma, epilepsy, multiple sclerosis, or other major neurological disorders.
- Malignant tumors. Family history of genetic disorders.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Yantai Yuhuangding Hospital
Yantai, Shandong, China
Yantai Yuhuangding Hospital
Yantai, China
Related Publications (1)
McKhann GM, Knopman DS, Chertkow H, Hyman BT, Jack CR Jr, Kawas CH, Klunk WE, Koroshetz WJ, Manly JJ, Mayeux R, Mohs RC, Morris JC, Rossor MN, Scheltens P, Carrillo MC, Thies B, Weintraub S, Phelps CH. The diagnosis of dementia due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimers Dement. 2011 May;7(3):263-9. doi: 10.1016/j.jalz.2011.03.005. Epub 2011 Apr 21.
PMID: 21514250BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chief Physician, Department of Neurology
Study Record Dates
First Submitted
May 6, 2026
First Posted
May 14, 2026
Study Start
January 16, 2026
Primary Completion (Estimated)
January 1, 2029
Study Completion (Estimated)
January 1, 2029
Last Updated
May 14, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
IPD will not be shared due to privacy regulations, ethical requirements, and limitations specified in the informed consent document.