Efficacy of a Multicomponent Cognitive Intervention in Adults With Subjective Cognitive Decline and Mild Cognitive Impairments
Efficacy of a Multicomponent Cognitive Intervention Program on the Cognitive and Daily Function in Adults With Subjective Cognitive Decline and Mild Cognitive Impairments: A Pilot Study
Individuals with mild cognitive impairment (MCI) and subjective cognitive decline (SCD) have greater risk of developing dementia. Cognitive intervention is a topic of great interest in individuals with MCI and SCD for the purpose of preventing or delaying the occurrence of dementia. There are many different types of cognitive interventions, which aim to positively impact the cognitive functioning of an individual and have been classified as cognitive stimulation, cognitive training, and cognitive rehabilitation. However, most studies used neuropsychological cognitive measures for outcome evaluation. The impact of cognitive interventions on daily functional performance among individuals with MCI and SCD were rarely explored. In addition, cognitive training focusing on specific cognitive outcomes is suspected to have limited far transfer to everyday measures. Therefore, a multicomponent intervention which integrates several types of intervention is recommended to reach the maximum impact on daily function.
The purposes of this study are to examine the effects of a multicomponent cognitive intervention on cognitive and daily functional outcomes in individuals with MCI and SCD, and to compare the effects between the two groups. In addition, the investigators will also investigate whether the demographic (e.g., age and educational level, etc.) and clinical variables (e.g., duration of cognitive complains, level of depression and baseline cognitive function, etc.) may affect the outcomes of cognitive intervention.
研究概览
详细说明
This study is a pretest-posttest design. Thirty-five subjects with MCI and 35 with SCD, who are diagnosed by physicians, will be recruited from the neurology outpatient clinic of National Taiwan University Hospital. All participants will wait for 16 weeks as a historical control and then receive the multicomponent cognitive intervention. The intervention is composed of 14 weekly 1.5-hour group sessions and 2 individual sessions in a 4-month period.
The multicomponent cognitive intervention in this study is a combination of several approaches, including cognitive training, cognitive rehabilitation, lifestyle interventions, and psychological interventions. Cognitive training is an approach which trains patients by repeated practicing to optimize or restore cognitive functions. Cognitive rehabilitation is tailored programs in which therapist usually provides patient strategies focusing on specific activities of daily life. Lifestyle interventions educate and encourage individuals to make changes to their life to balance the risk and protective factors. The strategies can include regular physical exercise, healthy nutrition (i.e., Mediterranean diet), frequent participation in cognitively-stimulating activities, and reduction of smoking and heavy alcohol consumption. Psychological interventions target neuropsychiatric symptoms that are common among individuals with SCD and MCI (e.g., depression, anxiety, fatigue, poor sleep) and thus include relaxation exercises, mindfulness techniques, skills to manage stress and poor sleep, and cognitive behavioral techniques. By using the approaches above together, the investigators hope to improve participants' cognitive and daily function.
All participants will be assessed at four time points: before waiting period (A0), before the intervention (A1), right after the 16-week intervention (A2), and 16 weeks after the intervention (A3). The primary outcomes are the subjective and objective performance of activities of daily living, and the secondary outcomes are the cognitive performance on the neurological tests, anxiety, and depression.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
-
Taipei、台湾
- National Taiwan University Hospital
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- over 50 years old
- years of education > 6
- mild cognitive impairment or subjective cognitive decline diagnosed by physician
- the Barthel Index scored 100
- the Montreal Cognitive Assessment (MoCA) > 18
- the UPSA-Brief > 50
Exclusion Criteria:
- without concurrent major or significant psychiatric disorders
- severe physical diseases which might affect cognitive functions
- difficult to follow instructions due to visual or hearing impairments
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
---|---|
实验性的:multicomponent cognitive intervention
|
The intervention takes place in groups of 6-10 participants and is leaded by one occupational therapist. It includes 16 sessions, 90 minutes each. The first part of each session starts with a 15-minute review of previous homework or relaxation. The second part, which lasts 35 minutes, involves structured training with activity-sheets, board games, role-playing and computerized games. The third part, which lasts 30 minutes, is the lifestyle interventions. The instructor explains the generalization of the previous activities toward daily life, and introduces healthy lifestyles. Through group discussions, the therapist guides participants to develop solutions and strategies for their memory or cognition-related problems and application to daily life. The last 10 minutes are used to suggest homework. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
---|---|---|
Change from Baseline the Brief University of California San Diego (UCSD) Performance-Based Skills Assessment (UPSA-Brief ) (Traditional Chinese Version) at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
The UPSA-Brief, which consists of 2 subscales (communication and financial), is a useful performance-based functional outcome scale.
It has adequate psychometric properties, predicts residential independence, is sensitive to change, and requires only 10-15 minutes to administer.
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the Activities of Daily Living Questionnaire at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
The Activities of Daily Living Questionnaire (ADLQ) is an informant-based assessment of functional abilities in patients with probable Alzheimer disease and other forms of dementia.
The ADLQ measures functioning in six areas: self-care, household care, employment and recreation, shopping and money, travel, and communication.
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the Contextual Memory Test (CMT) at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
The CMT is used to objectively measure awareness of memory capacity, strategy use and recall in adults with memory dysfunction.
It assess 3 areas of memory including: awareness of memory capacity, recall of line-drawn items, and strategy use.
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the Miami Prospective Memory Test (MPMT) at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
The Miami Prospective Memory Test evaluates time-related and event-related prospective memory ability of older adults.
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the Everyday Memory Questionnaire (EMQ) at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
The Everyday Memory Questionnaire (EMQ) was developed as a subjective measure of memory failure in everyday life.
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the Cognitive Failure Questionnaire (CFQ) at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
The CFQ assesses the frequency with which people experienced cognitive failures in daily life.
|
baseline, 16th, 32nd and 48th week
|
次要结果测量
结果测量 |
大体时间 |
---|---|
Change from Baseline the Word Sequence Learning Test at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the Wechsler Memory Scale-3rd ed. (WMS-III) Logical Memory (LM) subtest at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the Wechsler Memory Scale-3rd ed. (WMS-III) Family Pictures (FP) subtest at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the Color Trails Test at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the Geriatric Depression Scale-Short Form (GDS-S) at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
baseline, 16th, 32nd and 48th week
|
Change from Baseline the State-Trait Anxiety Inventory-Situation (STAI-S) at 16 weeks, 32 weeks, and 48 weeks
大体时间:baseline, 16th, 32nd and 48th week
|
baseline, 16th, 32nd and 48th week
|
合作者和调查者
调查人员
- 首席研究员:Hui-Fen Mao、National Taiwan University Hospital
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
multicomponent cognitive intervention的临床试验
-
University of Illinois at ChicagoShirley Ryan AbilityLab; Oakland University; Access Living主动,不招人
-
University of Wisconsin, MadisonNational Cancer Institute (NCI); Northwestern University主动,不招人