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Evolving Methods to Combine Cognitive and Physical Training for Individuals With Mild Cognitive Impairment

11 июля 2019 г. обновлено: Chang Gung Memorial Hospital

Evolving Methods to Combine Cognitive and Physical Training for Individuals With Mild Cognitive Impairment: An Efficacy Study

This study aims to investigate and compare the intervention effects of combining exercise and cognitive training (either sequentially or simultaneously in a dual-task paradigm) in elderly with mild cognitive impairment. The investigators hypothesize that (1) both sequential and dual-task training can induce greater improvements in the outcome measures than single mode of training; (2) the improvement in cognitive functions and other outcomes may differ between the groups.

Обзор исследования

Статус

Завершенный

Условия

Вмешательство/лечение

Подробное описание

Background and study aims:

Mild cognitive impairment (MCI) or minor neurocognitive disorder is a syndrome defined as an intermediate stage between cognitively intact and clinically diagnosed dementia. The age-adjusted prevalence of MCI in Taiwan is approximately 18%, while women have higher prevalence for MCI than men. The progression rate from MCI to dementia ranges from 10 to 15% each year, and over 50% of the MCI population will develop into severe cognitive impairment or dementia in 5 years. Therefore, early detection of the individuals who manifest MCI and provide appropriate interventions may help reduce the burden of their caregivers and the medical expenses of the health-care system. Previous studies found that cognitive training or exercise has emerged as an important therapeutic approach for individuals with MCI. However, the intervention effects of combining exercise and cognitive training remain to be determined. Furthermore, whether exercise and cognitive training should be administered in sequential order or simultaneously is an important question to pursue. The overall goal of this study is to determine and compare the intervention effects cognitive training, exercise, and combining cognitive and exercise training in individuals with MCI.

Who can participate? Individuals with MCI.

What does the study involve? The participants will receive a total of 36 training sessions, and each session will contain 90 minutes of training. Training frequency will be 2-3 times per week for 12-18 weeks. All participants will received pretreatment test, post treatment test, and a 6-month follow-up test.

What are the possible benefits and risks of participating? The possible benefits include improvement in cognitive, physical, and daily functions. There are no risks for participating.

Where to conduct the study? The investigators anticipate recruiting a total of 80 participants from geriatric day care centers and nursing homes from multiple cities in Taiwan.

Тип исследования

Интервенционный

Регистрация (Действительный)

55

Фаза

  • Непригодный

Контакты и местонахождение

В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.

Места учебы

  • Тайвань
      • New Taipei City, Тайвань, 249
        • Baliexcelsior Nursing Home
      • Taichung, Тайвань, 412
        • Pine nursing home
      • Taipei, Тайвань, 11150
        • Zhishan community home
      • Taipei, Тайвань, 11165
        • Bailing clinics and nursing homes
      • Taipei, Тайвань, 111
        • Shihlin cum day care center
      • Taipei, Тайвань, 11443
        • Xihu day care center
      • Taipei, Тайвань
        • TaoSheng Nursing home
      • Taoyuan, Тайвань, 333
        • Chang Gung Memorial Hospital
      • Taoyuan, Тайвань
        • Chang Gung Memorial Hospital Taoyuan Branch

Критерии участия

Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.

Критерии приемлемости

Возраст, подходящий для обучения

20 лет и старше (Взрослый, Пожилой взрослый)

Принимает здоровых добровольцев

Нет

Полы, имеющие право на обучение

Все

Описание

Inclusion Criteria:

  1. able to follow instruction,
  2. clinical dementia rating (CDR) = 0.5 or 1,
  3. self- or informant-reported memory or cognitive complaint, and
  4. able to perform activities of daily living (Barthel Index ≥ 70).

Exclusion Criteria:

  1. recent myocardial infarction,
  2. heart failure,
  3. recent heart surgery,
  4. severe asthma,
  5. concomitant with other neurological disorders, or
  6. joint deformity that might prevents them performing exercise or cognitive training.

Учебный план

В этом разделе представлена ​​подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.

Как устроено исследование?

Детали дизайна

  • Основная цель: Уход
  • Распределение: Рандомизированный
  • Интервенционная модель: Параллельное назначение
  • Маскировка: Одинокий

Оружие и интервенции

Группа участников / Армия
Вмешательство/лечение
Активный компаратор: Cognitive training group (Cog)
The BrainHQ program will be used to train different cognitive functions of the participants. The participants will practice tasks that involve the abilities of visuospatial processing, attention, memory, language, and/or executive functions. The tasks will become more difficult as the participants progress in their abilities.
Поведенческий: Cognitive training
visuospatial, attention, memory, and executive abilities
Активный компаратор: Physical exercise group (PE)
The participants in this group participate in multimodal exercise programs including aerobic exercise, balance, and strength training. The entire exercise program for the PE group will contain 10 minutes of warm-up, 70 minutes of physical exercise, and 10 minutes of cool-down. The 70 minutes of exercise session will be break up into 2 to 3 parts, and the participants can rest as needed during the exercise period.
Поведенческий: Physical exercise
endurance, balance, and mobility
Экспериментальный: Sequential training group (Seq)
The participants in this group will first perform 45 minutes of physical exercise followed by 45 minutes of cognitive training. The physical exercise training will be similar to the programs used in the PE group. The entire exercise program for the PE group will contain 5 minutes of warm-up, 35 minutes of physical exercise, and 5 minutes of cool-down. The cognitive training will be implemented with BrainHQ similar to what has been described in the COG group.
Поведенческий: Cognitive training
visuospatial, attention, memory, and executive abilities
Поведенческий: Physical exercise
endurance, balance, and mobility
Экспериментальный: Dual-task training group (Dual)
In this group, the participants will be instructed to perform physical exercise and cognitive tasks simultaneously (e.g., math calculation while stepping). The difficulty of the cognitive tasks will increase as the participants improve in their performance.
Поведенческий: Cognitive training
visuospatial, attention, memory, and executive abilities
Поведенческий: Physical exercise
endurance, balance, and mobility

Что измеряет исследование?

Первичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Change scores of Montreal Cognitive Assessment (MoCA)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The MoCA will be used to assess general cognitive functions. It examines several cognitive domains with a total score of 30.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of Stroop test
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The Stroop test will be used to assess the processing speed, inhibition, set-shifting, and selective attention abilities. The participants will be tested under 2 conditions: congruent and incongruent conditions. In the congruent condition, the color ink of a word is consistent with the written color name; while the color ink differs from the written color name under the incongruent condition.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of Dual-task test
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The dual-task tests will be assessed to determine the ability for an individual to perform 2 tasks simultaneously. The investigators will assess the dual-task performance during walking and performing box and block test. The results of the dual-task tests will provide information regarding to whether the 2 tasks compete for the same class of neural resources or one of the tasks can be carried out automatically.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of Timed up and go (TUG) test
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The TUG test will be used to assess the mobility and dynamic balance ability. The participants will be required to stand up from a chair, walk 3 meters, turn around, then walk back to the chair, and sit down. The time to complete the TUG test has been shown to be a good indicator to detect potential fallers and frail elderly (Podsiadlo & Richardson, 1991). The test-retest reliability of TUG on individuals with cognitive impairment was excellent (Blankevoort, van Heuvelen, & Scherder, 2013).
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)

Вторичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Change scores of the Verbal Fluency Test
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Verbal fluency tests will be used to evaluate the semantic memory of the participants. The participants will be instructed to say as many words as possible from a given category (i.e., fruit or animal) in 1 minute. The validity, reliability, and normative performance of verbal fluency tests have been well-established (Harrison, Buxton, Husain, & Wise, 2000).
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the Useful Field of View (UFOV)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Useful field of view (UFOV) is the visual area over which useful information could be obtained at a quick glance without eye or head movements. This UFOV will be assessed with the BrainHQ program. The UFOV will assess the abilities of visuomotor processing speed, divided attention, and selective attention (Ball, Edwards, & Ross, 2007).
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the 30 second chair stand test (CST)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The 30 second chair stand test (CST) will be assessed to indicate the strength and endurance level of the lower extremities. The participants will be asked to stand up from a standardized chair and then sit down as many times as possible within 30 seconds. The feasibility and reliability of using CST in people with cognitive impairment have been established to be good (Blankevoort et al., 2013).
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the Chinese version of the International Physical Activity Questionnaires (IPAQ)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The Chinese version of the International Physical Activity Questionnaires (IPAQ) is an international measure for health-related physical activity. A short form of IPAQ will be used to assess changes in physical activity before and after intervention in this study. The reliability and validity of IPAQ has been established across 12 countries (Craig et al., 2003).
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the Barthel Index (BI)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Assess activities of daily living
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the Lawton Instrumental Activities of Daily Living Scale
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Assess activities of daily living.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the Disability Assessment for Dementia (DAD)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Assess activities of daily living.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the Quality of Life in Alzheimer's Disease Instrument (QoLAD)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The Chinese version of QoLAD will be used.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the Caregiver Burden Inventory (CBI)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The Chinese version of CBI will be used.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the Geriatric Depression Scale (GDS)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The Chinese version of short form GDS will be used.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the Community Integration Questionnaire (CIQ)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The CIQ measures items relevant to home integration, social integration, and productive activities.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of the ActiGraph GX3 accelerometers Change scores of the ActiGraph
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The actigraphy will be placed on the waist for a 3-day period immediately before and after the intervention. The participants will wear the actigraphy during all daily activities except for those that involve water (i.e., showering or swimming).
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of evaluating isometric knee flexors and extensors muscle strength
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The participant will be seated upright in a chair with back support, the knee will be placed in 90-degree flexion and the evaluator will stabilize the thing to eliminate synergistic movements. Participants will be asked to perform a maximal isometric contraction of knee flexion and extension with both lower extremities. The investigators will record the mean value of 3 attempts.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of using hand dynamometer to measure grip strength of both hand
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The participant is seated, with the elbow at 90-degree flexion. The investigators will record the mean value of 3 attempts.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of Wechsler Memory Scale - Third Edition (WMS-III)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The investigators will use the WMS-III subtests, including Faces Recognition (score range 0-48), Verbal Paired Associates (score range 0-32), Word Lists (0-48), and Spatial Span (0-32) to assess the immediate, delayed, and working memory tests. Higher scores indicated better performance for each subtest. The raw score of each subtest will also be transferred to standardized Z scores and summed to represent an index of general memory function.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
Change scores of Wechsler Adult Intelligence Scale - Third Edition (WAIS-III)
Временное ограничение: baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
The WAIS-III includes tests that evaluate cognitive functions in verbal comprehension, working memory, perceptual organization, and processing speed. The subtests that the investigators will use are the Digit Symbol-Coding (scores range 0-133) and Matrix Reasoning tests (0-26). The raw score of each subtest will also be transferred to standardized Z scores and summed to represent an index of general cognitive function.
baseline, posttest (an expected average of 3 months), follow-up (up to 9 months)
BDNF val66met genotype
Временное ограничение: baseline
Saliva samples will be collected at baseline to determine the Brain-Derived Neurotrophic Factor (BDNF) val66met genotype.
baseline

Соавторы и исследователи

Здесь вы найдете людей и организации, участвующие в этом исследовании.

Спонсор

Chang Gung Memorial Hospital

Публикации и полезные ссылки

Лицо, ответственное за внесение сведений об исследовании, добровольно предоставляет эти публикации. Это может быть что угодно, связанное с исследованием.

Общие публикации

Даты записи исследования

Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.

Изучение основных дат

Начало исследования (Действительный)

30 января 2015 г.

Первичное завершение (Действительный)

29 января 2018 г.

Завершение исследования (Действительный)

13 марта 2019 г.

Даты регистрации исследования

Первый отправленный

20 июля 2015 г.

Впервые представлено, что соответствует критериям контроля качества

29 июля 2015 г.

Первый опубликованный (Оценивать)

31 июля 2015 г.

Обновления учебных записей

Последнее опубликованное обновление (Действительный)

12 июля 2019 г.

Последнее отправленное обновление, отвечающее критериям контроля качества

11 июля 2019 г.

Последняя проверка

1 мая 2019 г.

Дополнительная информация

Термины, связанные с этим исследованием

Ключевые слова

Дополнительные соответствующие термины MeSH

Другие идентификационные номера исследования

  • 103-6651A3

Информация о лекарствах и устройствах, исследовательские документы

Изучает лекарственный продукт, регулируемый FDA США.

Нет

Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.

Нет

Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .

Клинические исследования Cognitive training

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