The Effects of Single Baduanjin and Elastic Band Exercises on VSWM in Elderly Individuals With MCI
The Effects of Single Baduanjin and Elastic Band Exercises on Visuospatial Working Memory in Elderly Individuals With Mild Cognitive Impairment
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前：chen qiu
- 電話番号：86+13964805297
- メール：q13964805297@163.com
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Include the elderly population aged between 60 and 74 years old.
- Includes individuals with cognitive impairments. The patients or informants report experiencing memory decline and having certain cognitive dysfunction (MoCA score = 18-25 points).
- Including individuals who have controlled diabetes and/or cardiovascular diseases to a stable state.
- Irregular exercise with the ability to complete a certain amount of physical activities.
- Normal vision and hearing.
Exclusion Criteria:
- Patients with moderate to severe cognitive impairment, mental illness or other neurodegenerative diseases (such as Parkinson's dementia, stroke, frontotemporal degeneration, vascular dementia, Lewy body dementia, etc.).
- Long-term or recent use of psychotropic drugs, drugs that affect physical activity ability, cholinergic inhibitors, etc.
- Regular exercise habit .
- There are serious muscle disorders, or there has been an injury to the lower limbs within the previous six months, making it impossible to stand for a long time or to stand at all.
- Severe cardiovascular disease.
研究計画
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：独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
介入なし：コントロール
|
|
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実験的：baduanjin
|
Perform the 30-minute Baduanjin exercise
|
|
実験的：Resistance band
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Perform 30 minutes of elastic band exercises
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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 |
|---|---|---|
|
visuo-spatial working memory
時間枠：From July 1, 2026, to September 1, 2026, the duration is two months.
|
The primary research outcome pertains to visuospatial working memory, which is measured through a visuospatial working memory task paradigm.
The specific paradigm is as follows: First, a "+" appears in the middle of a gray computer screen for 300 ms.
Second, a 4x4 grid matrix appears at the center of the screen for 2000 ms, with 5 small black squares randomly placed within the matrix.
Immediately afterwards, a blank screen is presented for 3000 ms.
During this period, the participants are required to mentally visualize the probe stimulus after rotating it 90° to the left (or right).
Subsequently, a 4x4 grid target stimulus is presented again for 4000 ms, and the participants need to make a judgment on the target stimulus, specifically whether it is the result of rotating the probe stimulus 90° to the left (or right), as shown in Figure 3.
The entire experiment lasts approximately 8 minutes.
|
From July 1, 2026, to September 1, 2026, the duration is two months.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
EEG power value
時間枠：The total duration was two months.
|
The testers adjusted the impedance to below 5kΩ and followed the 26-system electrode placement method specified by the International Federation of Electroencephalography.
They set Fp1, Fp2, F3, F4, F7, F8, Fc3, Fc4, C3, C4, Cp3, Cp4, P3, P4, Pz, O1, O2, Oz, Po3, Po4, T3, T4, T5, and T6 leads.
The ground electrode was set as GND, and the reference electrode was at the bilateral earlobe positions of A1 and A2.
After stabilization, they began to record the EEG signals for 5 minutes.
Using the toolbox, they filtered out data segments with obvious artifact interference.
They analyzed the EEG indicators, including frontal cortex δ-β2 (Fp1, Fp2, F3, F4, F7, F8, AF3, AF4, Fc3, Fc4), central cortex δ-β2 (C3, C4, Cp3, Cp4), parietal cortex δ-β2 (P3, P4, Pz), occipital cortex δ-β2 (O1, O2, Oz, Po3, Po4), and temporal cortex δ-β2 (T3, T4, T5, T6).
|
The total duration was two months.
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
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。