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临床试验/NCT00480220
NCT00480220已完成不适用

Specific Care and Assistance Plan for Alzheimer's Disease: Impact Study on Disease Progression and Management Modalities

University Hospital, Toulouse54 个研究点 分布在 1 个国家目标入组 1,200 人开始时间: 2003年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,200
试验地点
54
主要终点
Evaluate the efficacy of the specific care and assistance plan for Alzheimer's disease in a study randomised within each centre. The main aim of the care plan is to reduce loss of independence.

研究概览

简要总结

The main objective of this work is to assess the feasibility and efficacy of a specific Care and Assistance Plan for Alzheimer's disease (PLASA). The main outcome measure selected is incapacity in carrying out the basic activities of daily living, evaluated by the ADCS-ADL scale .

The PLASA was developed by a working group appointed by the Direction Générale de la Santé as part of the government programme of action on Alzheimer's disease (October 2001, Ministère de l'Emploi et de la Solidarité).

详细描述

It is estimated that at the present time about 50% of dependence in the elderly is related to dementias. Alzheimer's disease is the most common of these, and there are 100 000 new cases in France every year (Girard Report). Very often, once the diagnosis has been established these persons do not receive regular, codified follow-up, whereas Alzheimer's disease is a chronic disease which progresses over several years and leads to a variety of complications which must be identified and managed.

The main objective of this work is to assess the feasibility and efficacy of a specific Care and Assistance Plan for Alzheimer's disease (PLASA). The main outcome measure selected is incapacity in carrying out the basic activities of daily living, evaluated by the ADCS-ADL scale .

The PLASA was developed by a working group appointed by the Direction Générale de la Santé as part of the government programme of action on Alzheimer's disease (October 2001, Ministère de l'Emploi et de la Solidarité).

Methods The multicentre prospective study will be randomised within each centre. Study population: 1200 patients will be recruited in 20 French university hospitals and 40 general hospitals.

Inclusion criteria: Patients presenting mild to moderate Alzheimer's disease diagnosed by the NINCDS-ADRDA criteria (MMSE between 12 and 26), living at home and with an identified principal caregiver.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

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

  • patient seen in consultation in one of the centres participating in the study
  • patient with probable or possible AD according to NINCDS-ADRDA criteria
  • patient with an MMSE score between 12 and 26 (mild to moderate disease)
  • patient capable of understanding and responding to the evaluations made
  • patient who is not confined to bed or chair
  • patient living at home with an informal caregiver
  • informed consent of the patient (or legal representative) and of the caregiver agreeing to take part in the study.

排除标准

  • patient with an MMSE score of less than 12 or over 26
  • patient incapable of understanding and responding to the evaluations made
  • patient confined to bed or chair
  • patient living at home without an informal carer or in an institution
  • patient with a concomitant disorder threatening the vital prognosis at two years
  • patient with a dementia other than AD
  • patient already included in another research programme.

结局指标

主要结局

Evaluate the efficacy of the specific care and assistance plan for Alzheimer's disease in a study randomised within each centre. The main aim of the care plan is to reduce loss of independence.

时间窗: 2 years

次要结局

  • Impact of the care and assistance plan: - on the mode of the patient's admission to an institution - on utilization of assistance, support and healthcare services (RUD questionnaire) - and on overall clinical evaluation of change (ADCS-CGIC).(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (54)

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