Blood Pressure Responses to Different Exercise Modes in Coronary Artery Disease
The Blood Pressure Responses to Different Exercise Models in Patients With Coronary Artery Disease
The purposes of this study were to compare blood pressure responses of the same target heart rate on different exercise modes in patients with coronary artery diseases (CAD) and to compare the effects of blood pressure responses after exercise training.
The investigators will recruit 30 subjects with CAD who are referred to phase II cardiopulmonary rehabilitation exercise training. The subjects performed the treadmill or stationary bicycle exercise randomly.
調査の概要
詳細な説明
Considering cardiopulmonary rehabilitation intensity is often setting by heart rate clinically, and only few study focused on exercise responses patients with CAD, the purposes of this study were to compare blood pressure responses of the same target heart rate on different exercise modes in patients with CAD and to compare the effects of blood pressure responses after exercise training.
This is a crossover trial study. The investigators will recruit 30 subjects with CAD who are referred to phase II cardiopulmonary rehabilitation exercise training. After at least 3 times of familiar with the cardiopulmonary rehabilitation training machine, the subjects performed the treadmill or stationary bicycle and exercise to personalized target heart rate for 10 minutes, take a rest until the heart rate recover to the resting heart rate, and then repeated the exercise in another exercise mode. The test order will be random. After at least 12 times of cardiopulmonary rehabilitation training, the test will be performed again.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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-
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Taipei city、台湾、100
- National Taiwan University Hospital
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- patients with coronary artery diseases who are referred to phase II cardiopulmonary rehabilitation exercise training.
Exclusion Criteria:
- patients with non-coronary artery diseases
- atrial fibrillation
- neurological or musculoskeletal problems
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:他の
- 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 |
|---|---|
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実験的:patients with coronary artery diseases
The investigators will recruit 30 subjects with CAD who are referred to phase II cardiopulmonary rehabilitation exercise training.
After at least 3 times of familiar with the cardiopulmonary rehabilitation training machine, the subjects performed the treadmill or stationary bicycle and exercise to personalized target heart rate for 10 minutes, take a rest until the heart rate recover to the resting heart rate, and then repeated the exercise in another exercise mode.
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The test order will be random.
After at least 12 times of cardiopulmonary rehabilitation training, the test will be performed again.
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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 |
|---|---|---|
|
heart rate
時間枠:Change from baseline heart rate at 6 weeks
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heart rate
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Change from baseline heart rate at 6 weeks
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blood pressure
時間枠:Change from baseline blood pressure at 6 weeks
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blood pressure
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Change from baseline blood pressure at 6 weeks
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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 |
|---|---|---|
|
perceived exertion scale
時間枠:baseline and 6 weeks
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how effort the participant feel.
Range from 1to 10.
Higher values represent harder.
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baseline and 6 weeks
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heart rate variability
時間枠:baseline and 6 weeks
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heart rate variability
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baseline and 6 weeks
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その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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age
時間枠:baseline
|
questionnaire
|
baseline
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gender
時間枠:baseline
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questionnaire
|
baseline
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risk level of exercise
時間枠:baseline
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AACVPR Stratification Algorithm for Risk of Event.
Include high, moderate and low risk
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baseline
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co-morbidity
時間枠:baseline
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questionnaire
|
baseline
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medication
時間枠:baseline
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questionnaire
|
baseline
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level of exercise intensity
時間枠:baseline
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percent of heart rate reserve
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baseline
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協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
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。