AzTrials
AzTrials

Postural ControlNCT07812103

Water-Inertia-Based Dynamic Stability Training for Balance and Postural Control in Healthy Young Women

A study testing Water-Inertia-Based Dynamic Stability Training and Stable-Load Dynamic Stability Training in people with Postural Control and Dynamic Stability, run by Yuanyan Huang at 1 site in South Korea.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This randomized controlled study evaluated the effects of a 10-week dynamic stability training program using a mobile water load compared with a mass-matched stable load in healthy young women. Thirty participants were randomly assigned to either water-inertia-based unstable-load training or stable-load training. Read more about this study

Who is it for?
Ages 19 to 25 years, women onlyHealthy volunteers can take part
Conditions the study is for
Postural Control, Dynamic Stability
What is being tested?
Water-Inertia-Based Dynamic Stability Training and Stable-Load Dynamic Stability Training
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteSouth Korea
Study dates
5 Jul 2024to 20 Sep 2024
Phase
Interventional
Are there results?
None posted in the registry

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 19 to 25 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Female undergraduate students aged 19 to 25 years.
  • Generally healthy at the time of enrollment.
  • No surgery within the previous 6 months.
  • No congenital, neurological, vestibular, or musculoskeletal disorder affecting the foot, pelvis, or spine.
  • No participation in resistance training during the previous 12 months. Able and willing to participate in the 10-week supervised exercise intervention and study assessments.
  • Provided written informed consent to participate.

Who cannot join

  • Did not meet any of the inclusion criteria.
  • Participated in resistance training or functional training outside the study intervention during the 10-week study period.
  • Developed a health condition, injury, or other circumstance during the study that prevented safe participation in the prescribed exercise program or outcome assessments.

Trial locations and contacts

1 site in 1 country.

South Korea1 site
  • Busan University of Foreign Studies

    Busan

Other trials in South Korea

About this study

Official title: Effects of Water-Inertia-Based Dynamic Stability Training on Dynamic Balance and Single-Leg Postural Control in Healthy Young Women: A Randomized Controlled Trial

This randomized controlled study evaluated the effects of a 10-week dynamic stability training program using a mobile water load compared with a mass-matched stable load in healthy young women. Thirty participants were randomly assigned to either water-inertia-based unstable-load training or stable-load training. Both groups completed the same supervised exercises three times per week, using vests with the same total external mass; the main difference between groups was whether the load inside the vest was mobile or stable. Outcomes were assessed before training, after 5 weeks, and after 10 weeks. The study evaluated dynamic balance, postural sway during single-leg stance, and other physical-performance outcomes to determine whether mobile water loading produced different training adaptations from stable loading.

Read the detailed description

This study was designed to examine whether dynamic stability training performed with a mobile water-based external load produces different physical and postural adaptations from the same training performed with a mass-matched stable external load in healthy young women. The study used a randomized, parallel-group design.

Healthy female university students aged 19-25 years who had not participated in resistance training during the previous 12 months were recruited. After baseline assessment, 30 eligible participants were randomly assigned in a 1:1 ratio to an unstable-load training group or a stable-load training group.

Both groups completed the same supervised dynamic stability training program three times per week for 10 weeks, for a total of 30 training sessions. Each session lasted approximately 50 minutes. The exercise content, training frequency, session duration, set-repetition structure, rest intervals, vest mass, and any additional prescribed exercise loads were matched between groups. During the main training block, participants completed three sets of each exercise, with 12 repetitions per set during weeks 1-5 and 15 repetitions per set during weeks 6-10.

The unstable-load group trained while wearing an Aqua Vest containing a total external load of 5 kg, consisting of approximately 4 kg of water and a 1-kg vest. Because the water pouches were partially filled, the internal water could move during exercise and change the distribution of the external load. The stable-load group wore a mass-matched weighted vest containing approximately 4 kg of steel rods and a 1-kg vest. The steel rods were arranged to approximate the spatial distribution of the water pouches. Thus, the primary experimental difference between groups was the mobility of the external load rather than total vest mass or prescribed exercise content.

Assessments were conducted at baseline, after 5 weeks of training, and after 10 weeks of training. Dynamic postural control was evaluated using the Y-Balance Test. Participants completed reaching tasks in the anterior, posteromedial, and posterolateral directions while standing on one limb. The maximum valid reach distance in each direction was retained and normalized to limb length, and a composite score was also calculated.

Postural sway was evaluated during single-leg stance using force-platform-derived center-of-pressure measures under eyes-open and eyes-closed conditions. Eyes-open trials lasted 30 seconds and eyes-closed trials lasted 20 seconds. Center-of-pressure outcomes included total path distance and direction-specific root-mean-square displacement in the anteroposterior and mediolateral directions.

The broader study protocol also included lower-extremity physical-performance assessments. The registration record is intended to describe the original study protocol and design; individual publications arising from the study may focus on specific subsets of the collected outcomes.

The purpose of the comparison was to determine whether introducing load mobility through a water-filled vest, while keeping the prescribed exercise program and external mass closely matched, resulted in different adaptations from training with a stable weighted vest.

Being tested
Water-Inertia-Based Dynamic Stability Training, Stable-Load Dynamic Stability Training
Keywords
water-inertia loading, unstable-load training, healthy young women, dynamic stability training, dynamic balance, postural control, Y-Balance Test, center of pressure, single-leg stance

What participants receive

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

  • Water-Inertia-Based Dynamic Stability TrainingBehavioural

    Also called Unstable-Load Training (ULT), Aqua Vest Training

    Participants completed a supervised dynamic stability training program three times per week for 10 weeks (30 sessions), with each session lasting approximately 50 minutes. During training, participants wore a vest providing a total external load of 5 kg, consisting of approximately 4 kg of water in partially filled pouches and a 1-kg vest. Internal water movement allowed the external load distribution to change during exercise. Exercises were performed for three sets, with 12 repetitions per set during weeks 1-5 and 15 repetitions per set during weeks 6-10, with 30 seconds of rest between sets. Exercise content and any additional prescribed implement loads were matched to the stable-load intervention.

  • Stable-Load Dynamic Stability TrainingBehavioural

    Also called Stable-Load Training (SLT), Weighted Vest Training

    Participants completed the same supervised dynamic stability training program three times per week for 10 weeks (30 sessions), with each session lasting approximately 50 minutes. During training, participants wore a stable weighted vest providing a total external load of 5 kg, consisting of approximately 4 kg of steel rods and a 1-kg vest. The steel rods were arranged to approximate the spatial loading configuration of the water pouches used in the water-inertia intervention. Exercises were performed for three sets, with 12 repetitions per set during weeks 1-5 and 15 repetitions per set during weeks 6-10, with 30 seconds of rest between sets. Exercise content and any additional prescribed implement loads were matched between groups.

Study groups in NCT07812103
Study groupRoleWhat they receive
Water-Inertia-Based Unstable-Load TrainingExperimentalParticipants assigned to this arm completed a supervised 10-week dynamic stability training program three times per week while wearing an Aqua Vest with a total external load of 5 kg, consisting of approximately 4 kg of water and a 1-kg vest. The partially filled water pouches allowed internal water movement during exercise, creating a mobile external load. Exercise content, session duration, set-repetition structure, rest intervals, and any additional prescribed exercise loads were matched to the stable-load training arm.
Receives: Behavioral: Water-Inertia-Based Dynamic Stability Training
Stable-Load TrainingActive comparatorParticipants assigned to this arm completed the same supervised 10-week dynamic stability training program three times per week while wearing a mass-matched stable weighted vest with a total external load of 5 kg, consisting of approximately 4 kg of steel rods and a 1-kg vest. The steel rods were arranged to approximate the spatial loading configuration of the water pouches. Exercise content, session duration, set-repetition structure, rest intervals, and any additional prescribed exercise loads were matched to the unstable-load training arm.
Receives: Behavioral: Stable-Load Dynamic Stability Training

What is being measured

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

  1. Normalized Anterior Reach Distance on the Y-Balance Test

    Dynamic postural control was assessed using the lower-quarter Y-Balance Test. Participants performed three valid anterior reach trials while maintaining single-leg stance. The maximum reach distance was retained and normalized to the corresponding limb length: normalized reach distance (%) = maximum reach distance / limb length × 100. Higher values indicate greater normalized reach performance.

    Measured: Baseline, Week 5, and Week 10

  2. Normalized Posteromedial Reach Distance on the Y-Balance Test

    Participants performed three valid posteromedial reach trials during the lower-quarter Y-Balance Test. The maximum reach distance was retained and normalized to the corresponding limb length: normalized reach distance (%) = maximum reach distance / limb length × 100. Higher values indicate greater normalized reach performance.

    Measured: Baseline, Week 5, and Week 10

  3. Normalized Posterolateral Reach Distance on the Y-Balance Test

    Participants performed three valid posterolateral reach trials during the lower-quarter Y-Balance Test. The maximum reach distance was retained and normalized to the corresponding limb length: normalized reach distance (%) = maximum reach distance / limb length × 100. Higher values indicate greater normalized reach performance.

    Measured: Baseline, Week 5, and Week 10

  4. Y-Balance Test Composite Score

    The composite score was calculated from the maximum valid anterior, posteromedial, and posterolateral reach distances normalized to limb length: composite score (%) = (maximum anterior + maximum posteromedial + maximum posterolateral reach distance) / (3 × limb length) × 100. Higher values indicate greater overall Y-Balance Test performance.

    Measured: Baseline, Week 5, and Week 10

  5. Center-of-Pressure Total Distance During Eyes-Open Single-Leg Stance

    Postural sway was assessed using a force platform during 30-second eyes-open single-leg stance. Total CoP distance (cm) represented the cumulative path length of the center-of-pressure trajectory during each valid trial. Three trial-specific values were averaged for analysis. Lower values represent a shorter CoP trajectory during the test condition.

    Measured: Baseline, Week 5, and Week 10

  6. Anteroposterior CoP RMS During Eyes-Open Single-Leg Stance

    Anteroposterior root-mean-square (AP RMS) displacement of the center of pressure was calculated during 30-second eyes-open single-leg stance and expressed in centimeters. AP RMS represents the dispersion of CoP displacement about its mean position in the anteroposterior direction. Three trial-specific values were averaged for analysis.

    Measured: Baseline, Week 5, and Week 10

  7. Mediolateral CoP RMS During Eyes-Open Single-Leg Stance

    Mediolateral root-mean-square (ML RMS) displacement of the center of pressure was calculated during 30-second eyes-open single-leg stance and expressed in centimeters. ML RMS represents the dispersion of CoP displacement about its mean position in the mediolateral direction. Three trial-specific values were averaged for analysis.

    Measured: Baseline, Week 5, and Week 10

  8. Center-of-Pressure Total Distance During Eyes-Closed Single-Leg Stance

    Postural sway was assessed using a force platform during 20-second eyes-closed single-leg stance. Total CoP distance (cm) represented the cumulative path length of the center-of-pressure trajectory during each valid trial. Three trial-specific values were averaged for analysis. Lower values represent a shorter CoP trajectory during the test condition.

    Measured: Baseline, Week 5, and Week 10

  9. Anteroposterior CoP RMS During Eyes-Closed Single-Leg Stance

    Anteroposterior root-mean-square (AP RMS) displacement of the center of pressure was calculated during 20-second eyes-closed single-leg stance and expressed in centimeters. AP RMS represents the dispersion of CoP displacement about its mean position in the anteroposterior direction. Three trial-specific values were averaged for analysis.

    Measured: Baseline, Week 5, and Week 10

  10. Mediolateral CoP RMS During Eyes-Closed Single-Leg Stance

    Mediolateral root-mean-square (ML RMS) displacement of the center of pressure was calculated during 20-second eyes-closed single-leg stance and expressed in centimeters. ML RMS represents the dispersion of CoP displacement about its mean position in the mediolateral direction. Three trial-specific values were averaged for analysis.

    Measured: Baseline, Week 5, and Week 10

  11. Knee Extension Peak Torque Relative to Body Weight at 60°/s

    Concentric knee extension strength was assessed using an isokinetic dynamometer at an angular velocity of 60°/s. Peak torque was normalized to body weight and expressed as a percentage of body weight (PT/BW, %). Higher values indicate greater knee extensor torque relative to body weight.

    Measured: Baseline, Week 5, and Week 10

  12. Knee Flexion Peak Torque Relative to Body Weight at 60°/s

    Concentric knee flexion strength was assessed using an isokinetic dynamometer at an angular velocity of 60°/s. Peak torque was normalized to body weight and expressed as a percentage of body weight (PT/BW, %). Higher values indicate greater knee flexor torque relative to body weight.

    Measured: Baseline, Week 5, and Week 10

  13. Ankle Inversion Peak Torque Relative to Body Weight at 60°/s

    Concentric ankle inversion strength was assessed using an isokinetic dynamometer at an angular velocity of 60°/s. Peak torque was normalized to body weight and expressed as a percentage of body weight (PT/BW, %). Higher values indicate greater inversion torque relative to body weight.

    Measured: Baseline, Week 5, and Week 10

  14. Ankle Eversion Peak Torque Relative to Body Weight at 60°/s

    Concentric ankle eversion strength was assessed using an isokinetic dynamometer at an angular velocity of 60°/s. Peak torque was normalized to body weight and expressed as a percentage of body weight (PT/BW, %). Higher values indicate greater eversion torque relative to body weight.

    Measured: Baseline, Week 5, and Week 10

  15. Ankle Inversion Peak Torque Relative to Body Weight at 120°/s

    Concentric ankle inversion strength was assessed using an isokinetic dynamometer at an angular velocity of 120°/s. Peak torque was normalized to body weight and expressed as a percentage of body weight (PT/BW, %). Higher values indicate greater inversion torque relative to body weight.

    Measured: Baseline, Week 5, and Week 10

  16. Ankle Eversion Peak Torque Relative to Body Weight at 120°/s

    Concentric ankle eversion strength was assessed using an isokinetic dynamometer at an angular velocity of 120°/s. Peak torque was normalized to body weight and expressed as a percentage of body weight (PT/BW, %). Higher values indicate greater eversion torque relative to body weight.

    Measured: Baseline, Week 5, and 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 posted10 Sep 2026
  2. Study start5 Jul 2024
  3. Primary completion20 Sep 2024
  4. Study completion20 Sep 2024

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
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07812103
Sponsor's protocol ID
2024-0666-001
Other IDs
P01-202407-01-004
Status last verified
Sep 2026
First submitted
4 Sep 2026
Last updated
14 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: De-identified individual participant data that support the findings of the study may be shared with qualified researchers upon reasonable request, subject to applicable ethical and data-protection requirements.

Questions about this trial

What is this clinical trial studying?

A study testing Water-Inertia-Based Dynamic Stability Training and Stable-Load Dynamic Stability Training in people with Postural Control and Dynamic Stability, run by Yuanyan Huang at 1 site in South Korea.

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: finished, as of the sponsor's last update on 14 Sep 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 South Korea. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Normalized Anterior Reach Distance on the Y-Balance Test (time frame: Baseline, Week 5, and Week 10). The study lists 16 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 14 Sep 2026.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in