Multicomponent Exercise Training in Frail Elderly
Effectiveness of the Multicomponent Exercise Training in Frail Elderly
The aim of the present study will be to assess the effectiveness of the multicomponent exercise training in frail for the physical function, frailty and performance.
All the individuals will be assessed two times.
調査の概要
詳細な説明
This will be a experimental, randomized controlled intervention study in frail. Subjects will be recruited at the Albertia Care Center, Madrid. The exercise training group will developed a concurrent training 3 days per week during 6 weeks. The control group will follow an usual care also for 6 weeks.
The main variables will be as follows:
- Ultrasound imaging measurements for the lower limb: core muscles, vastus medialis, rectus femoris, vastus intermedius, gastrocnemius, soleus. We will employed a General Electric (GE) Ultrasound device in B mode to assess the thickness of the muscles.
- Heart rate variability with a Suunto smart bell.
- Activities of daily living with the Bartel index.
- Force-velocity profile and muscle power.
- Frailty with the Linda´s frailty criteria.
The exercise program was applied for 6 weeks. A total of 18 sessions were distributed in 3 weekly sessions. The participants performed a resistance exercises: leg press at an intensity of 40%-60% with 10 repetitions, 12 repetitions of steps with their bodyweight and a plantar flexion followed by a cardiovascular high intensity interval training (HIIT) exercise walking on a treadmill.
One measurements will be taken (pre), the second (post) measurements will be performed at 6 weeks.
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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Madrid、スペイン
- Albertia Elderly Care Center
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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:
- Men and women aged 75 years or more,
- 2 or more points in the Short Physical Performance Battery (SPPB)
- Capability of walking (alone or assisted)
Exclusion Criteria:
- Severity cognitive alterations
- Severe disability on the Barthel score
- Surgeries in the previous 6 months
- Other any disorder that exclude for the exercise group.
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 |
|---|---|
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実験的：Exercise program
The exercise program was applied for 6 weeks.
A total of 18 sessions were distributed in 3 weekly sessions.
The participants performed a resistance exercises: leg press at an intensity of 40%-60% with 10 repetitions, 12 repetitions of steps with their bodyweight and a plantar flexion followed by a cardiovascular HIIT exercise walking on a treadmill.
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A multicomponent exercise program
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アクティブコンパレータ：Daily activities
The patients who belongs to this group will continue to perform their daily routines.
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A multicomponent exercise program
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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 |
|---|---|---|
|
Thickness of the core and quadriceps muscles
時間枠：Change from baseline muscle thickness at 6 weeks
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Thickness assessment by ultrasound imaging
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Change from baseline muscle thickness at 6 weeks
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Heart rate variability
時間枠：Change from baseline heart rate variability at 6 weeks
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Heart rate variability by Suunto smart bell device
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Change from baseline heart rate variability at 6 weeks
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Daily life activities
時間枠：Change from baseline daily life activities at 6 weeks
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Bartel index questionnaire
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Change from baseline daily life activities at 6 weeks
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Muscle power
時間枠：Change from baseline muscle power at 6 weeks
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Force-velocity profile for the lower limb muscle power
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Change from baseline muscle power at 6 weeks
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Frailty
時間枠：Change from baseline frailty at 6 weeks
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Frailty with the Linda´s frailty criteria
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Change from baseline frailty at 6 weeks
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協力者と研究者
捜査官
- 主任研究者：Sergio López, MsC、Universidad Europea de Madrid
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。