Cognitive Regulation Training and Exercise Trial (CORTEX-II)
2020年12月7日 更新者：Sean Mullen、University of Illinois at Urbana-Champaign
Cognitive Regulation Training and Exercise (CORTEX)-II With Middle-Aged Adults
The purpose of this double-blinded, randomized controlled study is to compare CORTEX (Cognitive Regulation Training and Exercise), a multi-faceted, center- and home-delivered- general and exercise-specific-active and traditional computerized cognitive training (CT) program to an attention-control condition involving health and wellness informational videos.
More specifically, the cognitive training group will emphasize dual-task abilities, working memory, and visual-spatial processing, as well as self-as-exerciser priming and self-certainty training.
It is hypothesized that early intervention cognitive training will enhance use of self-regulatory strategies and self-efficacy and in turn, increase exercise adherence to and engagement in a 12-month aerobic and resistive exercise program at a local fitness facility.
More positive improvements in cognitive and psychosocial functioning among participants in the CORTEX condition (relative to the Video Attention-Control condition, i.e., health educational videos), are also expected immediately following the cognitive training, and across time.
Expectancies and knowledge of study purpose (blinding integrity) will also be measured and used to statistically adjust for any training differences.
調査の概要
詳細な説明
Primary Aim: To test the effectiveness of a 1-month CT (randomized group condition) on exercise self-regulation, a latent factor representing 12-Month exercise adherence & program engagement (i.e., supervised & unsupervised class participation rates, electronically-recorded visitations, Fitbit-derived step counts, & self-reported leisure-time exercise), the investigators will use a structural equation model with robust maximum likelihood estimation. Exercise self-regulation will be regressed on group and known covariates (age, gender, education level, training compliance [percentage of completed sessions], and injury/illness). It is hypothesized that the CORTEX condition will show increased exercise self-regulation (and lower dropout, a categorical outcome variable, tested in a parallel model) compared to the Video Attention-Control condition.
Secondary Aims: A generalized latent variable framework will be used to test the researchers' theorized model and exploratory questions to determine if the CT contributes to greater cognitive change and enhanced perceptions of memory strategy use, self-efficacy, and self-reported physical activity-specific planning and self-regulatory strategy-use; and in turn, greater exercise self-regulation/ lower dropout. To evaluate these questions, first and second-order latent change scores will be derived representing general & exercise-specific cognitive functioning (reaction times and accuracy within training domains), self-efficacy and self-reported self-regulatory strategies, and will be added to the latent exercise self-regulation measurement model (and adjusted with known covariates, i.e., group, age, gender, education, compliance, injury/illness). Positive indirect effects of CT condition on 12-month exercise self-regulation are expected through the change in theoretical constructs-dual task and memory performance, implicit attitudes, memory strategy-use, self-efficacy, exercise planning and physical activity-specific self-regulatory strategy-use. Researchers also predict that the CT program will demonstrate high feasibility/acceptability, as indicated by a thorough process evaluation.
研究の種類
介入
入学 (実際)
233
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
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Illinois
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Urbana、Illinois、アメリカ、61801
- University of Illinois
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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
35年～64年 (大人)
健康ボランティアの受け入れ
はい
受講資格のある性別
全て
説明
Inclusion Criteria:
- Men and women
- Low active for the past 3 months
- 35 to 64 years old
- Do NOT regularly play exergames (e.g., XBox Kinect, Playstation Move, Nintendo Wii)
- Do NOT engage in "brain training" regularly (less than once per week)
- Are NOT enrolled in another exercise program or cognitive training study
- Able and willing to comply with the study length, testing, training and exercise program requirements
- Lives within 20 miles of the fitness facility and UIUC research facility
- Has reliable at-home Wi-Fi internet access and an available port for plugging in XBox console
- Vision is at least 20/40 with glasses or contacts with no color blindness
- Do NOT have depression (as defined by a score of 2 or less on the abbreviated Geriatric Depression Scale [GDS-5])
- Do NOT have cognitive impairment (as defined by a score of 21 or higher on the Telephone Interview Cognitive Survey [TICS])
Exclusion Criteria:
- Previously involved in the first CORTEX trial
- Currently involved in regular weekly cognitive training or another physical activity program or study (e.g., yoga, meditation)
- Too active (as defined by regularly exercise 2 or more days per week for 30+ minutes over the past 3 months)
- Incapable of performing moderately intensive aerobic exercise (must be able to complete basic movements, i.e., walking, jogging, jumping, side-stepping, throwing, kicking, punching, grabbing) without exacerbating a pre-existing condition caused by overuse, surgery, or other chronic condition
- Unable or unwilling to comply to lab and home-based training and physical activity prescription
- Unable to commit to full length of program
- Unwilling to be randomized to one of two groups
- Home residence exceeds 20 mile radius from fitness facility or unable to commute to and from fitness facility and UIUC campus
- Do not have reliable at-home Wi-Fi internet access or a required port for plugging in Xbox
- Uncorrectable vision (i.e., less than 20/40 with glasses or contacts with color blindness)
- Depression as defined by GDS >2
- Cognitive impairment as defined by TICS < 21
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：ランダム化
- 介入モデル：並列代入
- マスキング：トリプル
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的：Gaming Condition
The games group will visit the lab on 5 separate occasions, for 2 hours each, to complete training sessions (playing seated and standing computerized games), and then complete 5 similar sessions at home (lasting 2 hours, but may be split into 1-hour sessions at their convenience), at the onset of the exercise program.
The training sessions will be scheduled concurrently with exercise classes in the first month.
This group will also be asked to accumulate 150 minutes of exercise by attending weekly supervised and unsupervised, group-based aerobic and resistance exercise classes, by visiting the fitness facility alone, and by walking or strength training at home when necessary to supplement fitness facility activities to fully meet public health recommendations, for a period of 12 months.
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The game training will emphasize general and exercise-specific dual task processing, self-priming and certainty training.
他の名前：
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アクティブコンパレータ：Video Condition
The videos group will visit the lab on 5 separate occasions, for 2 hours each, to view health and educational YouTube videos, and then view 5 similar sessions at home (lasting 2 hours, but may be split into 1-hour sessions at their convenience), at the onset of the exercise program.
The training sessions will be scheduled concurrently with exercise classes in the first month.
This group will also be asked to accumulate 150 minutes of exercise by attending weekly supervised and unsupervised, group-based aerobic and resistance exercise classes, by visiting the fitness facility alone, and by walking or strength training at home when necessary to supplement fitness facility activities to fully meet public health recommendations, for a period of 12 months.
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The video training will emphasize health and educational information.
他の名前：
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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 |
|---|---|---|
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Exercise self-regulation
時間枠：12 months
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Exercise self-regulation will be modeled within a latent variable framework.
The change factor will be reflected by accumulated supervised and unsupervised class participation rates, total electronically-recorded visitations, averaged monthly Fitbit-derived step counts, and self-reported leisure-time exercise (via Godin Leisure-Time Questionnaire).
Measures will be standardized as z-scores.
The latent factor model will be adjusted for known covariates (age, gender, education level, training compliance [percentage of completed sessions] and injury/illness) when primary hypothesis of group effects is tested.
There is always the possibility that attempts to analyze latent constructs will not converge as planned.
In such a case, researchers will attempt to assess change across each behavioral outcome individually with a robust linear regression method, adjusting for multiple comparisons.
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12 months
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Dual task functioning (change)
時間枠：1 month
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Four separate heterogeneous dual task transfer assessments will involve auditory and/or visual stimuli.
The tasks will progress from a focus on response to singularly-presented stimuli to dual task trials involving equally-prioritized responses (accuracy and quickness) to combinations of colors-letters, pictures-arrows, sounds-voices, and animals-planets.
The percentage of incorrect response trials, accuracy, and reaction time will be the outcome measures for each of these tasks.
Dual-task percent cost will then be calculated by the following equation: (dual task reaction time - single task reaction time) /single reaction time) x 100.
Cost scores will be included as latent factor indicators in a structural equation model testing change from baseline to 1-month follow-up (post-intervention).
Measures will be standardized as z-scores.
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1 month
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Memory functioning (change)
時間枠：1 month
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Again, from a latent factor perspective, multiple measures will be used to assess the construct of memory functioning, which will reflect overall working memory, spatial and episodic memory.
Assessments will be utilized from the iPad-delivered NIH Toolbox, as well computerized assessments developed in E-Prime (e.g., Sternberg).
Latent factor memory functioning change from baseline to 1-month follow-up (post-intervention) will be represented by total percent correct for each assessment at each time point.
Measures will be standardized as z-scores.
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1 month
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Exercise self-efficacy (change)
時間枠：1 month
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Once again, from a latent factor perspective, multiple measures will be used to assess confidence that one can successfully walk longer distances (Self-Efficacy for Walking Scale), continue an exercise regimen (Exercise Self-Efficacy Scale), accumulate physical activity into one's life (Lifestyle Self-Efficacy Scale) and overcome barriers (Barriers Self-Efficacy Scale).
An Exercise Self-Efficacy latent factor will be derived from equally-weighted latent factor indicators from each of the scales, and will be used to assess change in exercise-related efficacy beliefs from baseline to 1-month follow-up (post-intervention).
Measures will be standardized as z-scores.
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1 month
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Physical activity self-regulatory strategy-use (change)
時間枠：1 month
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Participants' perceived use of exercise-specific self-regulatory strategies will be assessed with the multi-dimensional 12-item Physical Activity Self-Regulation Scale.
Each of the 12 items will serve as the latent factor indicators for baseline and 1-month follow-up (post-intervention).
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1 month
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Exercise planning (change)
時間枠：1 month
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The 10-item Exercise Planning and Scheduling Scale will be used to assess change in exercise-specific planning behaviors from baseline to 1-month follow-up (post-intervention).
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1 month
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Memory strategy-use (change)
時間枠：1 month
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Again, from a latent factor framework, multiple self-report scales assessing memory strategy-use (subscale of Metamemory Questionnaire), memory self-efficacy (10-item Memory Self-Efficacy Scale), behavioral self-control (13-item Brief Self-Control Scale), affective and cognitive self-control (10-item Volitional Components Inventory) will be used to derive a latent factor to assess change in perceived Memory Strategy-Use from baseline to 1-month follow-up (post-intervention).
Measures will be standardized as z-scores.
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1 month
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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。
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)
2017年1月1日
一次修了 (実際)
2020年5月31日
研究の完了 (実際)
2020年10月10日
試験登録日
最初に提出
2017年4月6日
QC基準を満たした最初の提出物
2017年4月18日
最初の投稿 (実際)
2017年4月24日
学習記録の更新
投稿された最後の更新 (実際)
2020年12月10日
QC基準を満たした最後の更新が送信されました
2020年12月7日
最終確認日
2020年12月1日
詳しくは
本研究に関する用語
その他の研究ID番号
- 16447
- GRANT12053054 (その他の助成金/資金番号：National Institute on Aging)
- 1R01AG052707-01A1 (米国 NIH グラント/契約)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
はい
IPD プランの説明
Upon study completion and after publication of the primary aims and hypotheses, the investigators will provide de-identified data to any interested parties with the provision that they consult with the investigators about the study design, analytical procedures, and to avoid redundancy in future planned analyses or manuscripts.
The PI will be given priority and will work closely with other investigators in maximizing ways to leverage the data to address other research questions.
Data generated from this project will be made available in multiple formats with codebooks via NCBI's BioProject within 12 months of completing aforementioned priorities.
These include demographic information (e.g., age, gender, and education), group assignment codes, and outcome measures.
No personally identifying information will be included.
Users must also agree to the conditions of use governing access to the public release data.
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
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。
Gamesの臨床試験
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Foundation University Islamabad完了