Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
1400 participants
OBSERVATIONAL
2021-05-01
2026-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
1. The prevalence and characteristics of AD in South China's aging population
2. Identify novel biomarkers and neuroimaging techniques for early detection and intervention of AD
3. Supporting and fertilizing novel approaches and techniques for early diagnosis and intervention of AD Participants will undergo cognitive assessments, blood sample collection, and genetic testing. Some will undergo CSF collection, stool sample collection, MRI scanning, Aβ PET scanning, and tau PET scanning.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Exploring the Predicting Biomarkers From Mild Cognitive Impairment to Dementia (EBMID)
NCT05697588
Early Markers of Cognitive Change and Alzheimer s Disease
NCT01867346
Computerized Tests of Cognitive Decline in Presymptomatic Alzheimer's Disease
NCT04800588
Protein and microRNA Markers for Early Detection of Alzheimer's Disease
NCT03388242
Cognitive Impairment in Ageing People
NCT04360200
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
All the GHABS participants will undergo cognitive assessments, genetic screening, and blood sample collection. Some will have CSF collection, stool sample collection, MRI scanning, Aβ PET scanning, and tau PET scanning. All baseline examinations will be completed within three months. At follow-up, clinical assessments and blood sample collection will be conducted annually. CSF sample collection, MRI scan, Aβ PET scan, and tau PET scan are evaluated every two years.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Fluids biomarker and neuroimaging of AD diagnosis
Early diagnosis of Alzheimer's disease in South China aging population using fluids biomarker and neuroimaging.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* The score of the Geriatric Depression Scale (GDS) is less than 6 points.
* There is a caregiver who can maintain at least 10 hours of contact per week and can accompany volunteers to the test site for testing.
* Visual and auditory acuity is sufficient for neuropsychological testing. (Including normal corrected vision and hearing)
* Be in good health and are expected to be free of disease interference during the study.
* Volunteers are not pregnant, lactating or have reproductive potential (that is, women must be two years after menopause or undergo sterilization surgery).
* Willingness and ability to participate in longitudinal imaging studies.
* A modified version of the Hachinski Ischemic scores less than or equal to 4.
* Have completed grade 6 education or have good work experience (sufficient to rule out mental retardation).
* Must be able to speak Mandarin fluently.
* Willing to undergo multiple 3T MRI scans and at least two PET scans.
* Agree to collect blood for genomic analysis (including GWAS sequencing and other analyses), AD risk and protective genes such as apolipoprotein E (APOE), klotho, etc., and biological sample storage.
* Agree to collect blood for biomarker detection.
* Agree to share genomic data and biomarker samples.
Exclusion Criteria
* Any volunteers who do not meet the MRI scan requirements, including having a cardiac pacemaker, eyes, skin or metal fragments or foreign bodies in the body.
* Severe depression, bipolar affective disorder described in DSM-IV in the past year.
* Psychotic features, agitation or behavioral problems that may lead to difficulty complying with the protocol content in the past 3 months.
* Currently using medication to treat obsessive-compulsive disorder or attention deficit disorder.
* History of schizophrenia (meeting DSM-IV criteria).
* History of alcohol or drug abuse or dependence within the past 2 years (metting DSM-IV criteria).
* Any major systemic disease or unstable physical condition that may make longitudinal research difficult.
* Clinically significant abnormalities of B12 or TFTs may interfere with the study, low B12 will be excluded.
* Currently using certain psychoactive medications (e.g., certain antidepressants, neuro-depressants, chronic anxiolytics, or sedative-hypnotics). Currently using warfarin or other anticoagulants such as dabigatran, rivaroxaban, and apixaban (except lumbar puncture).
* Use of prohibited drugs.
* Simultaneously participating in other clinical studies involving neuropsychiatry.
55 Years
90 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Natural Science Foundation of China
OTHER_GOV
Guangdong Basic and Applied Basic Science Foundation
UNKNOWN
Shenzhen Science and Technology Innovation Commission
UNKNOWN
Shenzhen Bay Laboratory
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Tengfei Guo
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Tengfei Guo, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Shenzhen Bay Laboratory
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Shenzhen Bay Laboratory
Shenzhen, Other, China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Informed Consent Form
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
YL2023-001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.