Effect of LiFE-SePBT on Postural Stability in Community-dwelling Older Adults: an Assessor-blinded Randomised Controlled Trial (LiFE-SePBT)
Combined Effects of Lifestyle-integrated Functional Exercise and Self-initiated Perturbation-based Balance Training on Postural Stability in Community-dwelling Older Adults: an Assessor-blinded Randomised Controlled Trial
This study is an assessor-blinded randomised controlled trial investigating the effects of combined Lifestyle-integrated Functional Exercise and Self-initiated Perturbation-based Balance Training (LiFE-SePBT) on postural stability in community-dwelling older adults with an elevated risk of falling.
調査の概要
状態
詳細な説明
Participants will be randomly assigned to two groups: LiFE-SePBT or an attention control group. All participants will provide their written informed consent before baseline assessment. The study will be reported and conducted in line with the CONSORT statement. Participants will be recruited via convenience sampling in the local community. After baseline assessment, both groups will receive five 90-minute intervention sessions over 10 weeks. Between-group differences in behaviour will be examined before and after training to identify immediate training-induced changes in postural stability. Retention of the changes in postural stability will be assessed four months after the training period. Fall incidents will be followed up for 12 months after training.
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:Bryan Tsz Lok Heung, Bsc
- 電話番号:+852-9210-2491
- メール:26119566r@connect.poly.hk
研究場所
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Kowloon
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Hung Hom、Kowloon、香港、000
- 募集
- The Hong Kong Polytechnic University
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コンタクト:
- Bryan Tsz Lok Heung, Bsc
- 電話番号:+852-9210-2491
- メール:26119566r@connect.polyu.hk
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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:
- Community-dwelling older adults aged 60 or older
- Able to communicate effectively in Cantonese or Mandarin
- Able to walk independently on level ground for at least 30 minutes
- A score of ≥ 6 in the Abbreviated Mental Test (Hong Kong)
- Have fallen in the preceding year, have concerns about falling, or feel unsteady while walking or standing
Exclusion Criteria:
- Uncorrected vision or hearing impairment
- Osteoporosis
- Hip or knee replacement within the last year
- Resting blood pressure ≥ 160/100 mmHg even with medication taken
- A score of ≤ 6 in 5-items Geriatric Depression Scale (GDS-5)
- Have musculoskeletal, cardiovascular, mental, or neurological disorders that preclude their participation in the assessment or intervention safety
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:ランダム化
- 介入モデル:並列代入
- マスキング:ダブル
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:LiFE-SePBT
5 sessions of combined Lifestyle-integrated Functional Exercise and Self-initiated Perturbation-based Balance Training (LiFE-SePBT) will be delivered. The LiFE component involves having participants embed functional exercises into their lifestyle, as well as practising recovering their balance upon self-initiated perturbation. Each session is 90 minutes long and will be hosted once every 2 weeks. |
Lifestyle-integrated Functional Exercise and Self-initiated Perturbation-based Balance Exercise (LiFE-SePBT) is a synergistic fall prevention programme. LiFE programme targets generic balance and muscle strength whereas SePBT mainly influences through reactive balance. |
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プラセボコンパレーター:Attention control group
Participants in the attention control group will receive 5 sessions of upper limb mobilisation and flexibility exercises. Each session is 90 minutes long and will be held once every 2 weeks. |
Upper limb mobilisation and flexibility training, including arm circles, deltoid stretches, shoulder internal rotations, etc. |
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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Generic Balance ability
時間枠:Week 0 (baseline assessment), week 10 (post-assessment), week 22 (i.e., 3-month follow-up assessment)
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Generic balance ability will be assessed by the Mini-BESTest. Mini-BESTest can challenge balance across anticipatory postural adjustments, postural responses, sensory orientation and stability in gait, allowing for a comprehensive examination of improvements that occur in reactive control. |
Week 0 (baseline assessment), week 10 (post-assessment), week 22 (i.e., 3-month follow-up assessment)
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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 |
|---|---|---|
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Number of real-life falls
時間枠:1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, and 12 months after the intervention.
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The number of real-life falls in months after randomization will be recorded. Fall circumstances and related injuries will be required via phone contact. A fall is defined as an event resulting in a person unintentionally coming to rest on the ground or other lower level, not as the result of a major intrinsic event (e.g., syncope, stroke, or overwhelming hazard such as an earthquake). |
1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, and 12 months after the intervention.
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Dynamic balance
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Dynamic balance will be assessed by Alternative Step Test (in the unit of seconds). |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Balance confidence
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Balance confidence will be measured with the Chinese version of the shortened version of Activities-specific Balance Confidence Scale (ABC-6). The scale value is from 0 to 100, with higher values representing higher balance confidence. |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Functional lower body strength
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Functional lower body strength will be assessed by Five-time Sit to Stand Test (in the unit of seconds). |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Number of laboratory falls
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Participants will be exposed to one trip-like perturbation and slip-like perturbation on each foot at an unexpected time. The number of falls upon perturbations will be recorded. |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Depressive symptoms
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Depressive symptoms will be assessed by Five-Item Geriatric Depression Scale. Participants will be asked to answer 5 questions as yes or no. The answer "no" for the first question and "yes" for the other four questions will be evaluated for depression. |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Health-related quality of life
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Health-related quality of life will be assessed by the EQ-5D-5L. In the EQ-5D-5L descriptive system, each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. Each health state is identified by a five-digit code, with 11111 representing the best and 55555 the worst possible health state. |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Muscle activations
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Muscle activations will be assessed by surface electromyography using an electromyography system (Trigno IM, Delsys Inc., Natick, MA, USA). Fourteen electrodes are placed bilaterally over erector spinae, rectus abdominis, gastrocnemius medialis, biceps femoris, rectus femoris, tibialis anterior, and gluteus medius according to the SENIAM guidelines (www.seniam.org) by the physical therapist. |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Physical activity
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Physical activity will be assessed by the Physical Activity Scale for the Elderly. This questionnaire will ask participants to recall their activity over the last 7-days. Activity types include sitting, walking, sport/recreation, exercise, occupational and household. A total score for physical activity can be calculated using these answers and the predetermined weights associated with each activity. |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Cognitive flexibility and executive function
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Cognitive flexibility and executive function will be assessed by Trial Making Tests A and B (in the unit of seconds). |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Perceived ability to execute reactive stepping
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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The perceived ability to execute reactive stepping in different scenarios in real life situations via Short-Form Balance Recovery Confidence (SF-BRC) Scale. Each item is ranked from 0-10. |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Exercise adherence
時間枠:Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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Exercise adherence will be measured via the Chinese version of Exercise Adherence Rating Scale (EARS-C). The total score of this scale is ranked between 0 to 24; each item is graded from 0 to 4 while item 1, 4 and 6 are reverse-scored. |
Week 0, baseline assessment; Week 10, post-intervention assessment; Week 22, follow-up assessment.
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協力者と研究者
捜査官
- 主任研究者:Charlotte Sau Lan Tsang, PhD、The Hong Kong Polytechnic University
研究記録日
主要日程の研究
研究開始 (実際)
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
本研究に関する用語
キーワード
その他の研究ID番号
- HSEARS20260330008
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
Due to participant privacy concerns.
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