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NCT07891429Toboroz

Fuzhou Aging Brain Health Initiative

Fuzhou Aging Brain Health Initiative--Health Aging and Alzheimer's Disease Cohort and Early Diagnosis and Treatment Research

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. okt. 23.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

The goal of this observational study is to learn about the pathophysiological characterization and evolutionary patterns of Alzheimer's disease (AD) in older adults in Fujian Province, China. The primary purposes are as follows: 1. establishment and follow-up of cohorts in the general population and populations with cognitive impairment; 2. investigation of risk factors and evolutionary patterns of AD pathological characteristics; 3. construction and validation of AD digital phenotypes based on multi-dimensional digital-intelligence screening; 4. exploration of AD-related risk genes and their mechanisms of action; 5. development of novel technologies for plasma biomarkers and PET imaging for the accurate diagnosis of AD.

Állapot (regiszter)
Toboroz
Vizsgálattípus
Megfigyeléses
Résztvevők száma
3000 (tervezett)
Első benyújtás
2026. okt. 10.
Kezdés
2024. jan. 1.
Elsődleges befejezés
2036. aug. 31.
Fő szponzor
Fujian Medical University Union Hospital
Betegségek
Alzheimer-kór
NCT-szám
NCT07891429

Mit vállalsz

  • Vizsgálat típusa: Megfigyeléses
  • Tervezett résztvevők: 3000
  • 2024. jan. 1. és az elsődleges befejezés (2036. aug. 31.) között
  • 4 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

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Korábbi kezelés

  • Concomitant severe systemic diseases or unstable general medical conditions that would preclude participation in the longitudinal follow-up of this study;
  • Current use of psychoactive drugs, including antidepressants, neuroleptics, long-acting anxiolytics, or sedative-hypnotics; long-term use of anticoagulants such as warfarin, dabigatran, rivaroxaban, or apixaban (except for lumbar puncture procedures);
  • Concurrent participation in other neuropsychiatric clinical studies.

Más betegség

  • Coexisting severe neurological disorders, including Parkinson's disease, multi-infarct dementia, Huntington's disease, normal pressure hydrocephalus, intracranial tumors, progressive supranuclear palsy, epilepsy, subdural hematoma, multiple sclerosis, etc.; history of severe traumatic brain injury with persistent neurological deficits, or history of definite structural brain abnormalities;
  • Brain MRI findings indicating intracranial infection, cerebral infarction, focal organic lesions, or multiple lacunar infarcts in key memory-related brain regions;
  • Contraindications to MRI, such as implanted cardiac pacemakers, or the presence of metallic foreign bodies or fragments within the body;
  • Diagnosis of major depressive disorder or bipolar disorder according to DSM-5 criteria within the past 1 year; presence of psychotic symptoms, agitation, or aggressive behavior within the past 3 months that would preclude compliance with the study protocol;
  • Past history of schizophrenia, or current pharmacotherapy for obsessive-compulsive disorder or attention deficit disorder;
  • History of alcohol or substance abuse or dependence meeting DSM-5 criteria within the past 2 years;

Laborértékek

  • Clinically significant abnormalities in serum vitamin B12 or thyroid function indicators, with direct exclusion for those presenting with decreased vitamin B12 levels;

Kiket keres a vizsgálat

  • Age between 55 and 90 years, both sexes eligible;
  • Educational level of primary school or above, or with a sound working history, excluding individuals with intellectual disability;
  • Able to speak Mandarin fluently and capable of completing the full battery of neuropsychological assessments;
  • Geriatric Depression Scale (GDS) score ≤ 6;
  • Adequate visual and auditory function to complete all neuropsychological tests successfully;
  • Willing and able to provide peripheral blood samples and to undergo brain PET and MRI neuroimaging examinations;
  • If taking relevant medications, the dosage must have been stable for at least 4 weeks. Specific medication requirements: stable doses of antidepressants are permitted, provided that the participant has no significant anticholinergic adverse effects and no history of major depressive episode within the past year; estrogen replacement therapy is allowed; Ginkgo biloba preparations may be taken, but routine use is not recommended; use of any psychoactive drugs is prohibited within 4 weeks prior to screening.

Életkor a regiszterben: 55 év – 90 év · Nem: nők és férfiak · Egészséges önkénteseket is fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (4)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Fuqing City Gaoshan Town Health CenterFushunKínaToboroz
Huada Street Community Health Service CenterFuzhouKínaToboroz
Antai Street Community Health Service CenterFuzhouKínaToboroz
Fujian Medical University Union HospitalFuzhouKínaToboroz

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