集中的なコンピュータ認知トレーニングの影響 (CCT)
2026年9月28日 更新者：Kirk Daffner, MD、Brigham and Women's Hospital
コンピューター化された認知トレーニング: 後天性脳損傷における認知機能の向上を予測する要因の特徴付け
To investigate factors that predict cognitive enhancement following engagement in an intensive Computerized Cognitive Training Protocol.
調査の概要
詳細な説明
To investigate factors that predict cognitive enhancement following engagement in an intensive 6-month, 5 days per week training use the ABI Wellness BEARS platform and Brainex Software Symbol Relations Module.
The study will examine the impact of intensive working memory training on neurocognitive markers of brain plasticity (intervention-related changes) in 1) performance on neuropsychological tests, 2) BDNF levels in blood and salivary, 3) ERP measures of working memory, and 4) resting state fMRI and structural MRI.
研究の種類
介入
入学 (推定)
30
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
-
-
Massachusetts
-
Boston、Massachusetts、アメリカ、02115
- Brigham and Women's Hospital
-
-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
25年～65年 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
Inclusion Criteria:
- Patient of the Mass General Brigham Health System with primary attention and executive functioning difficulties and/or a diagnosis of mild cognitive disorder or mild neurocognitive disorder (non-amnestic profile), due to an acquired brain injury (ABI) sustained at least 12 months prior to study contact.
- Ages 25-65 years old
- Proficiency in English
- Willing and able to complete all study-related activities for 12 months, including travel to Brigham and Women's Hospital (Boston) for four in-person assessment visits and two serum and saliva sample collections.
- Access to a computer with webcam and stable internet.
- A reliable study informant who can complete one questionnaire about participant's cognition/daily functioning, at four time points.
Exclusion Criteria:
- History of alcohol or substance abuse, or dependence, within the past 2 years, as per DSM-5 criteria.
- High likelihood of an underlying progressive neurodegenerative disorder.
- Evidence of moderate to severe cognitive disorder, based on a score of 21 or less on the Mini-Mental Status Examination (MMSE) (Tombaugh & McIntyre, 1992).
- Patient Health Questionnaire (PHQ)-9 (Kroenke et al., 2010) Score ≥ 19, unless deemed by treating provider not to have active depression (e.g., adjustment disorder, grief reaction).
- Active psychotic symptoms.
- Severe sensory losses such that participants would unlikely be able to participate in the study training, even with substantial accommodations (self-report of extreme difficulty reading ordinary newspaper print or a performance-tested corrected vision test score of worse than 20/30).
- Communication difficulties that prevent the participant from effectively participating in this highly interactive study protocol (based on interviewer's rating of a person's ability to be understood and to understand others).
- Current participation in a pharmacological, or other interventional research trial.
- Life expectancy of < 2 years.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：処理
- 割り当て：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的：Computerized Cognitive Training
See section of intervention/treatment for additional information. |
Participants will log into ABI Wellness Platform five days per week (M-T-W-Th-F) and train using the Symbol Relations module for 45 to 60 minutes. Every other week, participants will meet with their training facilitator via zoom to review training progress and troubleshoot any training-related questions. |
この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Changes in cognitive outcome measures
時間枠：6 months
|
We will use age-corrected standard scores of the NIH toolbox Total Cognitive Composite, Fluid Intelligence Composite, and individual scores on RAVLT, Verbal Fluency, and Trailmaking Task as cognitive outcome measures. |
6 months
|
|
Changes in BDNF Levels in blood and saliva
時間枠：6 months
|
Using FUJIFILM high sensitivity ELISA kits and commercially available ELISA kits. |
6 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Self-report exercise and physical activity
時間枠：6 months
|
Physical Activity Scale for the Elderly (questionnaire). Measures walking, moderate, and vigorous activity. Zero lower limit, no upper limit. Higher values indicate more physical activity. |
6 months
|
|
Intervention-related changes in ERP measures, such as the P3 component (P3a and P3b)
時間枠：6 months
|
1) Measured in response to verbal and visual working memory tasks |
6 months
|
|
Intervention-related changes in resting state fMRI
時間枠：6 months
|
A group ICA analysis procedure will be applied to pre- and post-intervention rs-fMRI BOLD signal activity. Correlations will be explored between fMRI parameters, cognitive, and training data (e.g NIH toolbox Total Cognitive Composite, Fluid Intelligence Composite, Crystallized Composite, CCT engagement and progress). |
6 months
|
|
Quality of life self-report
時間枠：6 months
|
Flanagan Quality of Life Scale (questionnaire). Measures quality of life. Likert scale 0-112, higher values indicate higher quality of life. |
6 months
|
|
Sleep
時間枠：6 months
|
Medical Outcomes Study Sleep Scale (questionnaire) Likert scale measuring sleep quality and sleep problems index. 0-60 with greater values representing higher sleep quality and lower sleep problems. |
6 months
|
|
Anxiety
時間枠：6 months
|
Generalized Anxiety Disorder 7 Item Scale (questionnaire) Likert scale measuring severity of anxiety. 0-21 with greater values representing more severe anxiety. |
6 months
|
|
Depression
時間枠：6 months
|
Patient Health Questionnaire Depression Scale (questionnaire) Likert scale measuring the severity of depression. 0-24 with higher scores representing more severe depression. |
6 months
|
|
Self-report on impact of fatigue
時間枠：6 months
|
Modified Fatigue Impact Scale Likert scale on the impact of fatigue on one's physical, cognitive, and psychosocial activity. 0-84 with higher scores indicating a greater impact of fatigue on a person's activities. |
6 months
|
|
Feelings about cognitive/thinking skills
時間枠：6 months
|
Cognitive Self- Efficacy Questionnaire Likert scale on feelings people have about their cognition/thinking skills. 0-72 with a higher score indicating more positive feelings regarding the efficacy of ones cognitive/thinking abilities. |
6 months
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
協力者
捜査官
- 主任研究者：Kim C Willment, PhD、Brigham and Women's Hospital
- 主任研究者：Kirk R Daffner, MD、Brigham and Women's Hospital
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
一般刊行物
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便利なリンク
- <p>Experiences of individuals with acquired brain injury and their families interacting with community services: a systematic scoping review</p>
- <p>Tracking early decline in cognitive function in older individuals at risk for Alzheimer's disease dementia: the Alzheimer's Disease Cooperative Study Cognitive Function Instrument</p>
- <p>Capacity-limited resources are used for managing sensory degradation and cognitive demands: Implications for age-related cognitive decline and dementia</p>
- <p>Resting state fMRI: a personal history</p>
- <p>Opportunities and limitations of intrinsic functional connectivity MRI</p>
- <p>The Flanagan Quality Of Life Scale: evidence of construct validity</p>
- <p>Resting-State Functional Connectivity: Signal Origins and Analytic Methods</p>
- <p>Group physiotherapy provides similar outcomes for participants after joint replacement surgery as 1-to-1 physiotherapy: a sequential cohort study</p>
- <p>Mechanisms Underlying Age- and Performance-related Differences in Working Memory</p>
- <p>National Institutes of Health Toolbox Cognition Battery</p>
- <p>Neuropsychological functioning during the year following severe traumatic brain injury</p>
- <p>The Experiences of Relatives of People with Acquired Brain Injury (ABI) of the Condition and Associated Social and Health Care Services</p>
- <p>That which doesn't kill us can make us stronger (and more satisfied with life): the contribution of personal and social changes to well-being after acquired brain injury</p>
- <p>Psychosocial functioning during the year following severe traumatic brain injury</p>
- <p>Group dynamics in the rehabilitation of hemiplegic patients</p>
- <p>Differential Effects of Physical Exercise, Cognitive Training, and Mindfulness Practice on Serum BDNF Levels in Healthy Older Adults: A Randomized Controlled Intervention Study</p>
- <p>BDNF mediates improvement in cognitive performance after computerized cognitive training in healthy older adults</p>
- <p>The Patient Health Questionnaire Somatic, Anxiety, and Depressive Symptom Scales: a systematic review</p>
- <p>Modified Fatigue Impact Scale</p>
- <p>Changes in brain-behavior relationships following a 3-month pilot cognitive intervention program for adults with traumatic brain injury</p>
- <p>Resting-state brain networks: literature review and clinical applications</p>
- <p>Is Computerized Working Memory Training Effective in Healthy Older Adults? Evidence from a Multi-Site, Randomized Controlled Trial</p>
- <p>The Multidimensional Fatigue Inventory (MFI) psychometric qualities of an instrument to assess fatigue</p>
- <p>The ACTIVE study: study overview and major findings</p>
- <p>The mini-mental state examination: a comprehensive review</p>
- <p>A comparison of the cost-effectiveness of two types of occupational therapy services</p>
- <p>The measurement of participant-reported memory across diverse populations and settings: a systematic review and meta-analysis of the Multifactorial Memory Questionnaire</p>
- <p>Overview of the Spinal Cord Injury-Functional Index (SCI-FI): Structure and Recent Advances</p>
- <p>Changes in Neural Activity Underlying Working Memory after Computerized Cognitive Training in Older Adults</p>
- <p>Rey Auditory-Verbal Learning Test: structure analysis</p>
- <p>Cost-effectiveness of cognitive-behavioural therapy and drug interventions for major depression</p>
- <p>Acquired brain injury: combining social psychological and neuropsychological perspectives</p>
- <p>The Physical Activity Scale for the Elderly (PASE): development and evaluation</p>
- <p>Group therapy utilization in inpatient spinal cord injury rehabilitation</p>
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2023年10月1日
一次修了 (実際)
2025年12月5日
研究の完了 (推定)
2026年12月1日
試験登録日
最初に提出
2023年10月30日
QC基準を満たした最初の提出物
2023年11月8日
最初の投稿 (実際)
2023年11月14日
学習記録の更新
投稿された最後の更新 (実際)
2026年10月1日
QC基準を満たした最後の更新が送信されました
2026年9月28日
最終確認日
2026年9月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。