跳至主要内容
临床试验/NCT03894254
NCT03894254招募中不适用

Predictive Factors Associated With Impairment in Functional Autonomy in a Regional Real-life Cohort of Patients With Alzheimer's Disease or Related Disorders (ADRD)

Hospices Civils de Lyon5 个研究点 分布在 1 个国家目标入组 5,400 人开始时间: 2020年9月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
5,400
试验地点
5
主要终点
Functional autonomy level

研究概览

简要总结

The Alzheimer's disease or related disorders (ADRD) are among the most disabling diseases because of their main features such as cognitive impairment, loss of functional autonomy and behavioural disorders. In absence of current curative treatment, the identification of the predictive risk factors of progression of the disease, evaluated through its main symptoms, represents a major stake of public health. The Investigators aim at developing a regional database, which includes the patient medical records on a prospective basis, in collaboration with the medical and administrative staff and with the University hospital computer science departments.

The main objective is to study the predictive factors associated with change in functional autonomy level, measured every 6 to 12 months in centres across Region Auvergne Rhone-Alpes in France.

The real-life study population will consist in about 5400 patients with ADRD. The inclusion period will be of 3 years, the length of follow-up of each patient will be of 10 years max for a total study length of 13 years.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients aged 18 years and older, undergoing a medical visit in a memory center or neuro-cognition service
  • •Patients living at home or in housing
  • •Patients with memory impairment, at all stage of the disease

排除标准

  • •Patients in institution
  • •Patients under legal protection
  • •Patients with a hearing or visual impairment, which prevents carrying out examinations

研究组 & 干预措施

Patients with subjective cognitive complaint or neurocognitive

Experimental

: Real-life cohort patients with subjective cognitive complaint or neurocognitive disorders undergoing medical examination in memory centers, and for whom extensive evaluations will be performed for the study

干预措施: no intervention (Other)

结局指标

主要结局

Functional autonomy level

时间窗: from 6 months to 12 months interval

The Lawton Instrumental Activities of Daily Living (IADL)

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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