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