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Line Dancing With Blood Flow Restriction for Balance and Gait of Older Women (In-Person vs Online)

2026年9月30日 更新者:Concordia University, Montreal

Fall Risk and Fatiguability Following Community Line Dancing Classes for Older Women

Falls are a leading cause of injury-related hospitalization among older women. Age-related declines in gait speed and postural stability are known risk-factors for falls. While exercise is well-known to help maintain or improve these losses, only 24.4% of older Canadian women are considered physically active.

Dance can act as a fun and social way to engage older women in exercise. Line dancing in particular has been shown to improve gait speed, knee extensor strength and endurance; however high doses are needed to achieve gains. Clifford and colleagues found that program lengths of 24 hours are needed to effect change, while Merome and colleagues recommend 3 hours per week. These high training doses may not be feasible for participants or community centres who offer programming. The time to commute to classes, find parking and caregiver roles at home are all cited as barriers to physical activity. We also propose that BFR could be a novel addition to increase the physiologic strain of online dance classes, which we hypothesize have a lower intensity and thereby lead to less fitness adaptations. Online classes are of interest as they can serve to reduce barriers to physical activity often experienced by older adults in Canada.

  • We propose online dance classes have reduced efficacy in stimulating adaptations to gait speed, strength and endurance when compared to in-person classes.
  • We propose blood flow restriction (BFR) as a novel addition to dance classes in order to aid in reaching physiological overload in more efficient time-frame.

BFR works by partially reducing blood flowing in and out of working muscles, thereby reducing oxygen availability, promoting anaerobic energy pathways and keeping metabolites in the muscles for a longer time period. Numerous studies have confirmed that when combined with low-intensity exercise BFR is capable of producing similar strength gains as high-intensity exercise. Additionally, BFR is safe and has been widely used among older adults and individuals with various medical conditions, including cardiovascular conditions.

While the benefits of BFR for muscle strength and hypertrophy have been greatly studied, there is limited research on its effects on gait and postural stability. Additionally, there is minimal research on potential combinations of BFR with dance-based activity.

  • This study will examine the differences between online and in-person delivery of 90 minute line dance classes on the postural stability and gait of older females over 10-weeks.
  • This study will then investigate the effects of combining BFR with 10-weeks of 90 minute line dancing classes for the postural stability and gait of older females.

Finally, muscle oxygenation and kinematic analysis will be conducted to help provide insight into any potential changes in gait and postural stability.

The intervention will consist of 10-weeks of line dancing classes, during which half the groups will be randomized to wear elasticized BFR bands pulled tight to a 7/10 of perceived pressure. Classes will be once per week for 90 minutes and will include a warm-up, 4 pre-set choreographies and a cool down. Breaks will be provided throughout the class.

Assessments will occur at pre, mid and post.

Gait will be assessed during a 6-minute walk test. During the test, participants will be filmed from a sagittal view to obtain kinematics. They will also be asked to wear a heart-rate monitor and muscle oxygenation sensors on their lower limbs.

Postural stability will be assessed via 30-seconds of quiet standing on force plates in conditions of eyes open, eyes closed and foam. Participants will also be asked to wear an accelerometer on their upper back during the assessment to obtain correlation to force plate data.

Functional strength will be assessed using 30-second sit to stand (with a secondary timer to obtain 5 time sit to stand length) and the Calf-Raise Senior test. Dynamic balance and mobility will be evaluated using the Functional Reach Test, and the Timed Up and Go in both single and dual-tasks. Aerobic capacity will be measured using a 3 minute Step Test while the participant wears a heart-rate monitor and muscle oxygenation sensors.

Finally scales of fears of falling, social connectedness, and overall mental health will be collected.

It is expected that this study will have great practical implications as the accessibility of this program can provide opportunities to older adults from various remote locations to increase their levels of physical activity in a safe manner. The affordability may also aid in adoption by community health and recreation centers as an easy-to-implement program that helps to improve the postural stability and gait of older women, thereby promoting independence and quality of life.

調査の概要

研究の種類

介入

入学 (推定)

60

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Quebec
      • Montreal、Quebec、カナダ、H3G 1M8
        • 募集
        • Concordia University
        • コンタクト:
        • 主任研究者:
          • Emma H Chen
        • 副調査官:
          • Rudy Grief

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

60年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

女性

説明

Inclusion Criteria:

  • Female
  • Healthy older adults (60+ years old)
  • Comprehension of spoken English
  • Able to visit Concordia University for all testing sessions
  • No contraindication for physical activity from their physician
  • For online arm: Access to a device with a webcam, Zoom and stable internet

Exclusion Criteria:

  • Occurrence/onset of a stroke, vertigo, concussion or lower-extremity injury during the 10-week intervention period
  • Presence of venous thromboembolism, peripheral vascular disease or sickle cell anemia
  • Vacations during the study period

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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:階乗代入
  • 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
アクティブコンパレータ:Online dance classes without BFR

Participants will complete 10 weeks of beginner level line dancing classes, once per week for 90-minutes on Zoom. Classes are structured with a 10 minute warm-up that reviews basic line-dancing steps, 4 dances of choreography (32 counts that repeat throughout the whole song, no tags, primarily facing forward), followed by cool-down stretches.

アクティブコンパレータ:In-person dance classes without BFR

Participants will complete 10 weeks of beginner level line dancing classes, once per week for 90-minutes at a local community centre. Classes will follow the same structure as the online program.

実験的:Online dancing with BFR

Participants will complete 10 weeks of beginner level line dancing classes, once per week for 90-minutes on Zoom. Classes are structured with a 10 minute warm-up that reviews basic line-dancing steps, 4 dances of choreography (32 counts that repeat throughout the whole song, no tags, primarily facing forward), followed by cool-down stretches.

Participants in the BFR group will be asked to wear 5 centimetre elasticized BFR bands on their proximal thighs at a 7/10 of perceived tightness during the dance classes.

実験的:In-person dancing with BFR

Participants will complete 10 weeks of beginner level line dancing classes, once per week for 90-minutes at a local community centre. Classes will follow the same structure as the online program.

Participants in the BFR group will be asked to wear 5 centimetre elasticized BFR bands on their proximal thighs at a 7/10 of perceived tightness during the dance classes.

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
Gait Speed
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Changes in gait speed during a 6 Minute Walk Test reported as m/s.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Postural Stability
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Change postural stability during 30 second trials of quiet standing (conditions: eyes open, eyes closed, foam). Forceplate data will be processed according to recommendations by Quijoux and colleagues (2021) postural sway will be reported in cm.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Functional Strength - Sit to Stand
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Changes in repetitions on 30 second Sit-to-Stand.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Functional Strength - Calf Strength
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Changes repetitions on the Calf Raise Senior Test.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

二次結果の測定

結果測定
メジャーの説明
時間枠
Aerobic Capacity - Muscle Oxygenation
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Changes in the slope, peaks and plateaus of participant's muscle oxygenation monitors during a 3 minute aerobic step test and 1 minute recovery period. The monitors will be worn on the participants gastrocnemius muscles and their vastus lateralis. Reported as %SmO2.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Gait - Muscle Oxygenation
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Changes in the slope, peaks and plateaus of participant's muscle oxygenation monitors during the 6 Minute Walk Test. The monitors will be worn on the participants gastrocnemius muscles and their vastus lateralis to gait insight into oxygen delivery and consumption during walking. Reported as %SmO2.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Aerobic Capacity - Heart Rate
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Changes in the slope, peaks and plateaus of participant's heart rate during a 3 minute aerobic step test and 1 minute recovery period. Participants will also be wearing muscle oxygenation monitors on their gastrocnemius muscles and on their vastus lateralis.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Gait - Heart Rate
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Changes in the slope, peaks and plateaus of participant's heart rate during the 6 Minute Walk Test. The monitors will be worn around the participant's chest while walking.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Gait - Kinematics
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Changes in participant's step length and cadence during the 6 Minute Walk Test will be reported. The parameters will come from a camera placed sagittally during the 6 Minute-Walk Test.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Mobility
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Participants will be asked to complete the Timed Up and Go test in 3 conditions (single task, cognitive dual-task counting backwards by 3s, mobility dual-task holding water). The time to do each will be reported.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Dynamic Balance
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Participants will be asked to complete a standing Functional Reach Test and the distance in cm will be recorded.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Survey - Number of Falls
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Participants will be asked to report any falls during the intervention period. The number of falls experienced will be reported.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Survey - Fear of Falls
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Participants will be asked to complete the Falls Efficacy Scale-International scale. Min score = 16, max score = 64. A higher score of 64 indicates a severe concern about falling.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Survey - Balance Confidence
時間枠:Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).

Participants will be asked to complete the Activities-Specific Balance Confidence Scale. Min score = 0, Max score = 100. 100 indicates complete confidence in the ability to maintain balance.

Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).
Surveys - Social Participation
時間枠:Comparing pre-testing (week 0) and post-testing (week 10).

Participants will be asked to complete the Self-efficacy for Social Participation scale (12-item). A total score of 0 indicates not confident at all, while a maximum score of 36 indicates complete confidence.

Comparing pre-testing (week 0) and post-testing (week 10).
Surveys - Social Support
時間枠:Comparing pre-testing (week 0) and post-testing (week 10).

Participants will be asked to complete the Duke Social Support Index (11-item). Minimum score of 11 indicates low connectedness while a maximum of 33 indicates greater perceived social support.

Comparing pre-testing (week 0) and post-testing (week 10).
Surveys - Depression
時間枠:Comparing pre-testing (week 0) and post-testing (week 10).

Participants will be asked to complete the Geriatric Depression Scale: Short Form. Min score = 0, max score = 15. A higher score indicates greater likelihood of depression.

Comparing pre-testing (week 0) and post-testing (week 10).
Surveys - Anxiety
時間枠:Comparing pre-testing (week 0) and post-testing (week 10).

Participants will be asked to complete the Geriatric Anxiety Inventory. Min score = 0, Max score = 20. I higher score indicates greater feelings of worry or anxiety.

Comparing pre-testing (week 0) and post-testing (week 10).

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2025年9月1日

一次修了 (推定)

2027年6月1日

研究の完了 (推定)

2027年7月1日

試験登録日

最初に提出

2026年8月26日

QC基準を満たした最初の提出物

2026年9月30日

最初の投稿 (実際)

2026年10月6日

学習記録の更新

投稿された最後の更新 (実際)

2026年10月6日

QC基準を満たした最後の更新が送信されました

2026年9月30日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 30020985

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