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Older WomenNCT07860541

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

A study testing Wearing blood flow restriction, Online dance classes and In-person dance classes in people with Older Women and Older Adults, Balance, run by Concordia University, Montreal at 1 site in Canada.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 60 years and older, women onlyHealthy volunteers can take part
Conditions the study is for
Older Women, Older Adults, Balance, Older Adults
What is being tested?
Wearing blood flow restriction, Online dance classes and In-person dance classes
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteCanada
Study dates
1 Sep 2025to 1 Jul 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 60 years and older
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Canada1 site, 1 recruiting
  • Concordia University

    Montreal, Quebec, H3G 1M8

    Andreas Bergdahl, 514-848-2424 ext. +3372, andreas.bergdahl@concordia.ca

    Emma H Chen

    Recruiting

Other trials in Canada

About this study

Official title: 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.

Read more
  • 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.

Being tested
Wearing blood flow restriction, Online dance classes, In-person dance classes
Keywords
blood flow restriction, line dancing, dance, tele-kinesiology, gait speed, postural stability

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Wearing blood flow restrictionOther

    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.

  • Online dance classesOther

    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.

  • In-person dance classesOther

    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.

Study groups in NCT07860541
Study groupRoleWhat they receive
Online dance classes without BFRActive comparatorNot described
Receives: Other: Online dance classes
In-person dance classes without BFRActive comparatorNot described
Receives: Other: In-person dance classes
Online dancing with BFRExperimentalNot described
Receives: Other: Wearing blood flow restriction; Other: Online dance classes
In-person dancing with BFRExperimentalNot described
Receives: Other: Wearing blood flow restriction; Other: In-person dance classes

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Gait Speed

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

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

  2. Postural Stability

    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.

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

  3. Functional Strength - Sit to Stand

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

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

  4. Functional Strength - Calf Strength

    Changes repetitions on the Calf Raise Senior Test.

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

Secondary outcomes (14)
  1. Aerobic Capacity - Muscle Oxygenation

    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.

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

  2. Gait - Muscle Oxygenation

    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.

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

  3. Aerobic Capacity - Heart Rate

    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.

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

  4. Gait - Heart Rate

    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.

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

  5. Gait - Kinematics

    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.

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

  6. Mobility

    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.

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

  7. Dynamic Balance

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

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

  8. Survey - Number of Falls

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

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

  9. Survey - Fear of Falls

    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.

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

  10. Survey - Balance Confidence

    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.

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

  11. Surveys - Social Participation

    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.

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

  12. Surveys - Social Support

    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.

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

  13. Surveys - Depression

    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.

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

  14. Surveys - Anxiety

    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.

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Oct 2026
  2. Study start1 Sep 2025
  3. Primary completion1 Jun 2027 (estimated)
  4. Study completion1 Jul 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Factorial
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07860541
Sponsor's protocol ID
30020985
Status last verified
Jul 2026
First submitted
26 Aug 2026
Last updated
6 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Wearing blood flow restriction, Online dance classes and In-person dance classes in people with Older Women and Older Adults, Balance, run by Concordia University, Montreal at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Andreas Bergdahl (514-848-2424 ext. 3372, andreas.bergdahl@concordia.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Gait Speed (time frame: Comparing pre-testing (week 0) to mid-testing (week 5) and post-testing (week 10).). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Oct 2026.

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