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

30 settembre 2026 aggiornato da: 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.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

60

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Quebec
      • Montreal, Quebec, Canada, H3G 1M8
        • Reclutamento
        • Concordia University
        • Contatto:
        • Investigatore principale:
          • Emma H Chen
        • Sub-investigatore:
          • Rudy Grief

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

60 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

Sì

Sessi ammissibili allo studio

Femmina

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Prevenzione
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione fattoriale
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: 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.

Comparatore attivo: 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.

Sperimentale: 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.

Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Gait Speed
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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).

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Aerobic Capacity - Muscle Oxygenation
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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).

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 settembre 2025

Completamento primario (Stimato)

1 giugno 2027

Completamento dello studio (Stimato)

1 luglio 2027

Date di iscrizione allo studio

Primo inviato

26 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

30 settembre 2026

Primo Inserito (Effettivo)

6 ottobre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

30 settembre 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 30020985

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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