JPRN-jRCTs031210534招募中未知
Elucidation of the mechanism of progression of preclinical Alzheimer's disease by a longitudinal imaging and biomarker cohort study - PAD-TRACK
iimi Yoshiki0 个研究点目标入组 170 人开始时间: 2022年1月5日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 170
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 50age old 至 <= 85age old(—)
- 性别
- All
入选标准
- •1) Provide written informed consent by free will.
- •2) If eligibility is qualified, consents to all study procedure is provided.
- •3) With diagnosis of not dementia and Global Clinical Dementia Rating (CDR) score of 0 or 0.5.
- •4) Age of ranging from 50 to 85 years at the time of informed consent.
- •5) Has a study partner that is willing to participate as a source of information and has approximately weekly contact with the participant (contact can be in-person, via telephone or electronic communication).
- •6) Approximately healthy without severe current or past medical history which hinder research participation.
- •7) With sufficient eyesight and hearing to undergo neuropsychological examinations.
- •8) Has sufficient Japanese ability for neuropsychological tests and questionnaires.
- •9) If a female participant has not undergone sterilization or is within 2 years of menopause: a pregnancy test before amyloid PET is negative.
- •10) Demonstrate a brain amyloid PET increase above the intermediate (subthreshold) level by the central amyloid PET judgement. The amyloid test result before the screening stage is available, in such case an approval of the principal investigator and PET core is required.
排除标准
- •1) Current medical history such as Alzheimer's disease, Parkinson's disease, cerebrovascular dementia, Huntington's disease, normal pressure hydrocephalus, brain tumors, progressive supranuclear palsy, epilepsy, subdural hematoma, multiple sclerosis, or history of head trauma with neurological deficit or a structural brain abnormality.
- •2) History of major depressive disorder or bipolar disorder defined by the DSM-V within the past year at the time of consent, or history within 3 months of psychosis, agitation, or behavior problem which interfere study protocol.
- •3) Have a history of schizophrenia defined by the DSM-V.
- •4) Have a history of alcohol or substance use disorder defined by DSM-V within 2 years.
- •5) In the unstable medical condition judged by the principal investigator that pose risks or that interfere research result or subject's performance. It includes uncontrolled hypertension, uncontrolled diabetes, clinically serious heart, lung, kidney, liver, endocrine, or systemic disease.
- •6) With an ineligibility judged by the research doctor
研究者
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