Four-Week Multicomponent Exercise Program in Older Adults
Effects of a 4-Week Multicomponent Exercise Program on Physical Function and Body Composition in Older Adults: A Non-Randomised Controlled Trial
This study evaluated the effects of a four-week supervised multicomponent exercise program on physical function and body composition in older adults. Participants were allocated non-randomly to an intervention group or a control group based on their ability to attend the scheduled training sessions. The intervention group completed eight supervised 30-minute exercise sessions over four weeks, while the control group maintained their usual daily activity and did not begin a new exercise program. Physical function, muscle strength, gait, static balance, body mass, and body composition were assessed at baseline and after four weeks.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
This prospective, non-randomised controlled intervention study investigated the effects of a short-term multicomponent exercise program in older adults. Participants were allocated to either an intervention group or a control group according to their ability to attend the scheduled training sessions, primarily based on logistical factors such as place of residence and travel feasibility.
The intervention consisted of eight supervised 30-minute training sessions performed twice weekly for four weeks. The program included exercises targeting muscle strength, mobility, balance, coordination, and functional performance. Exercise volume was progressively increased during the second half of the intervention by increasing the number of repetitions and sets.
The control group received no additional exercise intervention and was instructed to maintain usual daily activity and not initiate a new exercise program during the study period. Assessments were performed at baseline and after four weeks and included muscle strength, functional mobility, gait, static balance, body mass, and body composition.
研究の種類
研究の種類
入学 (実際)
入学
段階
段階
- 適用できない
連絡先と場所
研究場所
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-
-
Gorzów Wielkopolski、ポーランド、66-400
- Poznan University of Physical Education, Faculty of Sport Sciences in Gorzow Wielkopolski
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参加基準
適格基準
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:
Age 55-90 years Ability to ambulate independently without assistance from another person Ability to complete the full study protocol, including baseline and final assessments and, for the intervention group, participation in the four-week exercise program Provision of written informed consent
Exclusion Criteria:
Medical contraindications to physical exertion Cardiovascular, respiratory, neurological, or musculoskeletal conditions that could prevent safe performance of the tests or exercises Musculoskeletal injury or surgery within the previous six months Substantial balance or gait impairments requiring continuous assistance from another person Cognitive impairment preventing comprehension of instructions
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：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）
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的：Multicomponent Exercise
Participants completed a four-week supervised multicomponent exercise program consisting of eight 30-minute sessions performed twice weekly. |
A supervised four-week multicomponent exercise program comprising eight 30-minute sessions performed twice weekly. The program included handgrip squeezing with a soft ball, hip flexion with a resistance band, glute bridges, single-leg stance with multidirectional reaching, supine trunk rotation, cervical spine mobility exercises, and stepping over an obstacle. The program was divided into two stages, with progression during weeks 3-4 achieved by increasing the number of repetitions and sets. |
|
介入なし：Control
Participants received no additional exercise intervention between assessments and were instructed to maintain their usual daily activity levels and not begin a new exercise program. |
この研究は何を測定していますか？
主要な結果の測定
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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Change in Handgrip Strength
時間枠：Baseline to 4 weeks
|
Change in mean bilateral handgrip strength measured with a digital hand dynamometer, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Isometric Hip Flexion Strength
時間枠：Baseline to 4 weeks
|
Change in mean bilateral isometric hip flexion strength measured using an EasyForce dynamometer, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Isometric Hip Extension Strength
時間枠：Baseline to 4 weeks
|
Change in mean bilateral isometric hip extension strength measured using an EasyForce dynamometer, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Timed Up and Go Test Time
時間枠：Baseline to 4 weeks
|
Change in time required to complete the Timed Up and Go test, expressed in seconds. |
Baseline to 4 weeks
|
|
Change in Step Length
時間枠：Baseline to 4 weeks
|
Change in mean bilateral step length measured using the Zebris FDM-THQ instrumented treadmill, expressed in cm. |
Baseline to 4 weeks
|
|
Change in COP Sway Area
時間枠：Baseline to 4 weeks
|
Change in center-of-pressure sway area measured during 30-second quiet standing using a dual-plate posturographic platform, expressed in mm². |
Baseline to 4 weeks
|
|
Change in Body Mass
時間枠：Baseline to 4 weeks
|
Change in body mass measured using bioelectrical impedance analysis, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Estimated Muscle Mass
時間枠：Baseline to 4 weeks
|
Change in estimated muscle mass measured using bioelectrical impedance analysis, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Fat Mass
時間枠：Baseline to 4 weeks
|
Change in fat mass measured using bioelectrical impedance analysis, expressed in kg. |
Baseline to 4 weeks
|
|
Change in Bone Mass
時間枠：Baseline to 4 weeks
|
Change in estimated bone mass measured using bioelectrical impedance analysis, expressed in kg. |
Baseline to 4 weeks
|
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)
研究開始
一次修了 (実際)
一次修了
研究の完了 (実際)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
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
その他の研究ID番号
- AWF-SENIORS-44024
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?
IPD プランの説明
De-identified individual participant data underlying the reported results are available from the corresponding author upon reasonable request.
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。