跳至主要内容
临床试验/NCT03991806
NCT03991806进行中(未招募)不适用

Association of Centre of Excellence Self-Administered Questionnaire (CESAM) Score and Frailty Levels With Incident Health Adverse Events in Older Community Dwellers: Results of the Canadian Longitudinal Study on Aging

Jewish General Hospital1 个研究点 分布在 1 个国家目标入组 30,000 人开始时间: 2020年5月31日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
30,000
试验地点
1
主要终点
Dementia

研究概览

简要总结

This study evaluates the frailty and the health adverse events in the population of the Canadian Longitudinal Study on Aging. It will be used the Centre of Excellence Self-Administered questionnaire (CESAM) which assesses frailty of older adults by providing a score and a of frailty in 4 levels.

详细描述

Age is broadly recognized to confer a risk for health adverse outcomes, but it is an insensitive and non-specific measure for use in individual decision-making. Frailty has been emerging to take its rightful place as a better measure for over past decades. Despite general consensus that the concept of frailty is clinically useful, the lack of agreement on its definition and the challenge of its measurement by front-line health providers mean that frailty remains only 'their apparent' to chronological age as a criterion to select older persons at risk.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Being 65 years and over
  • Being enrolled in the Canadian Longitudinal Study on Aging

排除标准

  • Never being enrolled in the Canadian Longitudinal Study on Aging
  • Undisclosed health adverse events

结局指标

主要结局

Dementia

时间窗: around 18 months

The algorithm is a three- step process involving administration of the neuropsychological battery to develop composite score in the three domains-memory, executive function, and psychomotor speed. The primary outcome of the study will be to determine the number of participants to whom the memory, the executive function, and the psychomotor speed are affected.

次要结局

  • Medication(around 18 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Olivier Beauchet

MD, Professor of Geriatrics

Jewish General Hospital

研究点 (1)

Loading locations...

相似试验