Quality Assessment of a Training Period for Physical and Mentally Disabled People
調査の概要
詳細な説明
This study aimed at making a quality assessment of a 8 week training period for adults with physical and mental disabilities. A control group was added to compare the effect of the training with no training. Before the training period the participants were tested in relation to their physical status: weight, height, fat%, blood pressure, Aastrand test, chair stand test and waist circumference. In addition to this, the participants were instructed to wear an accelerometer to measure step and active minutes for 2-3 days a work.
The staff at the day center, where the participants works in daytime, were responsible for the physical training 2 times/week for 8 weeks. The training was an hour of combined aerobic, strength, balance and flexibility training.
The participants were tested after the training period using the same test-protocol as before.
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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Aalborg、デンマーク、9220
- Department of Physiotherapy, University College of Northern Jutland
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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:
- User of the centers included in the study
- Being able to stand alone
- Being able to use an exercise bike
- Being able to understand danish
Exclusion Criteria:
- Pregnancy
- Pacemaker
- Not being able to stand up by themselves
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：防止
- 割り当て：非ランダム化
- 介入モデル：並列代入
- 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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他の：Intervention
The participants in this group participated in exercise two times/week for 8 weeks
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Training two times/week for an hour each time in 8 weeks.
The training included strength training, aerobic training, balance training and flexibility training.
The training was modified to the participants and initiated by the staff at the center.
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介入なし：Control
The participants in the control group were instructed to maintain their daily routines.
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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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Body mass index
時間枠：Through study completion, an average of 8 weeks
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weight (kg)/height (m) x height (m)
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Through study completion, an average of 8 weeks
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Blood pressure
時間枠：Through study completion, an average of 8 weeks
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Diastolic pressure (mmHg) Systolic pressure (mmHg)
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Through study completion, an average of 8 weeks
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Completed chair stands
時間枠：Through study completion, an average of 8 weeks
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Number of completed chair stands
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Through study completion, an average of 8 weeks
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Aastrand test
時間枠：Through study completion, an average of 8 weeks
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Bike test to measure the physical fitness.
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Through study completion, an average of 8 weeks
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Waist circumference
時間枠：Through study completion, an average of 8 weeks
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Measured in cm
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Through study completion, an average of 8 weeks
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Physical activity
時間枠：During test session - 2-3 days
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Number of steps and active minutes
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During test session - 2-3 days
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協力者と研究者
協力者
捜査官
- スタディディレクター：Dorte Drachmann, Msc、University College of Northern Jutland, Denmark. Department of Physiotherapy
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
本研究に関する用語
その他の研究ID番号
- FOU-UU-2018-001
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
米国FDA規制機器製品の研究
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。