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    【ChiCTR-TRC-12002622】A study on the effects of Integrated Attention training for healthy older Chinese adults

    基本信息
    登记号

    ChiCTR-TRC-12002622

    试验状态

    结束

    药物名称

    /

    药物类型

    /

    规范名称

    /

    首次公示信息日的期

    2012-10-26

    临床申请受理号

    /

    靶点

    /

    适应症

    subjective cognitive complaints but no clinical dementia

    试验通俗题目

    A study on the effects of Integrated Attention training for healthy older Chinese adults

    试验专业题目

    An exploratory study on the effects of Integrated Attention training for healthy older Chinese adults with subjective cognitive complaints but no clinical dementia

    申办单位信息
    申请人联系人
    申请人名称
    联系人邮箱
    联系人邮编

    联系人通讯地址
    临床试验信息
    试验目的

    This will be a single blind Randomized Controlled Trial of 6 months duration. Older Chinese adults /9aged 60 or above) with subjective cognitive complaints without dementia will be randomized into 2 intervention groups. The intervention groups comprised of Integrated Attention Training Group(A) and Psycoeducation Group (C). Each participant will participate in regular activities arranged by the participating elderly centres for first 3 months and practices at home for next 3 months.;Duration of intervention:Six months;Description / name of comparative treatments:Description of treatments 1. The integrated attention (A) training group will have training on different attention tasks. Basic elements will include practice of focused attention on internal cues, selective attention, divided attention and everyday functional tasks focus on attention. 2. The controlled (C) group will be received psychoeducation on different health related topics. Intervention schedule The intervention will be conducted in two phases. 1. Induction phase – There will be a total of 12 training (once weekly) sessions over a 12 week period. Each training session will last for 45 minutes including introduction and closing. 2. Intervention phase - After the induction course has been completed, subjects will be advised to practice the respective training for not less than 30 minutes per day, and not less than 3 days per week. A practice manual will be offered to participants to aid home practice. To booster adherence to program, the intervention instructors will provide a refresher lesson every month. A log book will be used to keep track of the adherence. Research staffs will phone up participants every two weeks to remind continuation of program.

    试验分类
    试验类型

    随机平行对照

    试验分期

    Ⅳ期

    随机化

    Random

    盲法

    /

    试验项目经费来源

    Nil

    试验范围

    /

    目标入组人数

    20

    实际入组人数

    /

    第一例入组时间

    2012-11-01

    试验终止时间

    1990-01-01

    是否属于一致性

    /

    入选标准

    1. Subjects aged 60 or above. 2. Subjective cognitive complaints, measured by abbreviated Memory Inventory for the Chinese.；

    排除标准

    1. Clinical diagnosis of dementia, according to DSM-Ⅳ 2. Had a chronic psychiatric illness or an acute episode of major depression 3. Taking a psychotropic or other medication known to affect cognition (e.g. benzodiazepines, anti-dementia medication, etc.) 4) Clinically depressed, assessed by the Hamilton Depression Rating Scale 5) Attending regular cognitive training or other intervention for brain health during the study period 6) History of major neurological deficit including history of stroke, transient ischemic attack or traumatic brain injury 7) Significant communicative impairments.；

    研究者信息
    研究负责人姓名
    试验机构

    Nil

    研究负责人电话
    研究负责人邮箱
    研究负责人邮编

    /

    联系人通讯地址

    Nil的其他临床试验

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    Department of Psychiatry, G/F, Multi-Centre, Tai Po Hospital, Tai Po, N.T., Hong Kong的其他临床试验

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