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临床试验/NCT01998711
NCT01998711已完成不适用

Memory Group Intervention for Mild Cognitive Impairment: Impact of a Memory Group for Older Adults Reporting Memory Difficulties.

Bayside Health2 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2004年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
62
试验地点
2
主要终点
Neuropsychological measures of memory and attention

研究概览

简要总结

Aims:

To evaluate the efficacy of a brief intensive intervention for persons with mild cognitive impairment, assisted by family members or friends. To equip persons with mild cognitive impairment with specific skills to prevent memory failures and improve the capacity of patients and families to cope with everyday memory difficulties.

详细描述

Participants:

The sample will consist of 60 families who have a family member reporting memory loss and who have recently been assessed within the Cognitive Dementia and Memory Service (CDAMS). Participants will include patients and a family member / close friend. The potential patient participants must have received a diagnosis of mild cognitive impairment following a comprehensive clinical assessment. They must also be English speakers, live in the community, have no evidence of significant visual or auditory impairment, and have no history of diagnosed alcohol or drug abuse or major psychological disorder. Potential family / friend participants are expected to be spouses or adult children.

Brief Description:

Patients and their carers will be assigned to either a 'brief intervention group' or a 'no intervention group'. Over 5 1 1/2 -hour weekly sessions, the brief intervention group will be taught a memory skills program which emphasises practical strategies for dealing with everyday memory problems. Interactive group discussion and 'take home' exercises are also included. The no intervention group will serve as a control group, and will receive only their usual care from the the memory clinic. At the completion of the study, the brief intervention will be offered to those in the no intervention group.

All participants will complete questionnaires about knowledge of memory techniques, common memory and behaviour problems and emotional health at pre-intervention, post-intervention and after a 3-month follow-up.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Single (Investigator)

入排标准

性别
All
接受健康志愿者

入选标准

  • Participant presents with memory complaint Objective memory impairment on neuropsychological tests Normal general cognitive function Adequate activities of daily living Fails to reach criterion for clinical dementia according to NINCDS-ADRDA guidelines Living in the community Absence of significant visual or auditory impairment English speaker -

排除标准

  • 未提供

研究组 & 干预措施

Memory group

Experimental

Memory training

干预措施: Memory group (Behavioral)

Control

No Intervention

Standard care

结局指标

主要结局

Neuropsychological measures of memory and attention

Self-report on memory performance in everyday activities

Informant report on memory performance in everyday activities

Informant report on use of strategies

Assessment of psychological wellbeing

Self-report on use of memory strategies

次要结局

未报告次要终点

研究者

发起方
Bayside Health
申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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