NCT07586501

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
260

participants targeted

Target at P75+ for all trials

Timeline
32mo left

Started Jan 2026

Typical duration for all trials

Geographic Reach
1 country

2 active sites

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress12%
Jan 2026Jan 2029

Study Start

First participant enrolled

January 16, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

May 6, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

May 14, 2026

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2029

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2029

Last Updated

May 14, 2026

Status Verified

May 1, 2026

Enrollment Period

3 years

First QC Date

May 6, 2026

Last Update Submit

May 8, 2026

Conditions

Keywords

Cognitive impairment, dementia, Alzheimer's disease, biomarker, brain MRI, neuroimaging, cognitive assessment, elderly populationParkinson's disease

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

Age55 Years - 75 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Location

Yantai Yuhuangding Hospital

Yantai, China

Location

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

Cognitive DysfunctionParkinson DiseaseDementiaAlzheimer Disease

Condition Hierarchy (Ancestors)

Cognition DisordersNeurocognitive DisordersMental DisordersParkinsonian DisordersBasal Ganglia DiseasesBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesMovement DisordersSynucleinopathiesNeurodegenerative DiseasesTauopathies

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.

Locations