Effect of Squats on Postural Stability, Bilateral Coordination and Dynamic Balance

January 14, 2026 updated by: Lithuanian Sports University

IMMEDIATE EFFECTS OF SQUATS PERFORMED ON STABLE AND UNSTABLE SURFACES ON POSTURAL STABILITY, BILATERAL COMPARISON AND DYNAMIC BALANCE

The aim of this interventional study was to evaluate the immediate effects of a single bout of 30 squats performed on an unstable surface versus a stable surface on postural stability, bilateral coordination, and dynamic balance in healty subjects. We hypothesized that performing squats on an unstable surface would result in significantly greater improvements in these parameters compared to squats on a stable surface. By comparing the immediate effects under randomized conditions, this study seeks to contribute novel insights into the role of surface stability in acute exercise-induced balance adaptations.

Study Overview

Detailed Description

Despite the growing interest in instability training, there remains a lack of evidence regarding the acute effects of squats performed on stable versus unstable surfaces on key balance-related outcomes, including postural stability, bilateral coordination, and dynamic balance. Filling this gap is essential for informing clinical decision-making and optimizing performance and rehabilitation strategies. The study recruited young, relatively healthy, and physically active individuals-students (n = 42). Inclusion criteria were: 1) age between 18 and 35 years, and 2) voluntary consent to participate. Exclusion criteria were: 1) history of lower limb injury within the past six months, and 2) inability to maintain postural balance during testing.The study applied the following procedures: Participant Data Collection, Leg Length Measurement, Determination of Dominant Leg, Postural Stability Assesment, Dynamic Stability Assessment, and Bilateral coordination assessment.

All assessments were performed under controlled laboratory conditions by the same examiner to ensure reliability. Participants were instructed to avoid caffeine, strenuous exercise, and alcohol consumption for at least 12 hours prior to testing. and their hands placed on their hips.

Participants performed 30 bodyweight squats while standing with their feet shoulder-width apart and their hands placed on their hips. Each squat was executed to approximately 90° of knee flexion at the lowest point. The movements were paced using a metronome, with participants completing 30 squats within 45 seconds to ensure a consistent tempo and intensity.

The test was conducted under two conditions: on a stable surface and on an unstable surface, with a 48-hour interval between the two sessions.

Study Type

Interventional

Enrollment (Actual)

42

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Kauno M. Sav.
      • Kaunas, Kauno M. Sav., Lithuania, 44221
        • Department of health promotion and rehabilitation

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. age between 18 and 35 years,
  2. voluntary consent to participate in the study.

Exclusion Criteria:

  1. history of lower limb injury within the past six months,
  2. inability to maintain postural balance during testing.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Healthy student volunteers
42 students were tested under three conditions
Participants were tested without any exercise
Participants performed 30 squats on unstable surface before testing
Participants performed 30 squats on stable surface before testing

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Postural stability
Time Frame: Under three conditions (Condition 0, condition 1 an Condition 3) at least 48 hours apart

Individuals were asked to stand on the platform with both feet barefoot; the platform's instabil-ity level was set to 11 (with 11 representing a predefined setting on the system). Foot position was determined using the Biodex Balance System (BBS) platform, with the cuboid bones serv-ing as anatomical landmarks to ensure that the foot was centred; subjects' arms were positioned on their hips throughout testing. Postural stability tests were measured in 10-second trials with a 10-second rest period between tests, with a total of three trials conducted.

  1. Stability index (the lower the index, the better the stability). Overall stability index (Overall), sagittal plane's stability index (Forward/Backward) and frontal plane's stability index (Left/Right).
  2. Sway index (the lower the index, the lower the sway)
  3. Time in Zone (four zone sizes in percentage provided).
  4. Time in Quadrant (percentage of time).
Under three conditions (Condition 0, condition 1 an Condition 3) at least 48 hours apart
Bilteral Coordination
Time Frame: Under three conditions (Condition 0, condition 1 an Condition 3) at least 48 hours apart.

Using the Biodex machine the following parameters were measured:

  1. Sway index in sagittal plane (Anterior/Posterior direction) while standing on a left leg, hand placed on hips. Lower index meant greater results.
  2. Sway index in sagittal plane (Anterior/Posterior direction) while standing on a right leg, hands placed on hips. Lower index meant greater results.
  3. Differences in the sway index in the sagittal plane between the two legs. Lower index meant greater results.
  4. Sway index in frontal plane (Medial/Lateral direction) while standing on a left leg, hands placed on hips. Lower index meant greater results.
  5. Sway index in frontal plane (Medial/Lateral direction) while standing on a right leg, hands placed on hips. Lower index meant greater results.
  6. Differences in the sway index in the frontal plane between the two legs. Lower index meant greater results.
  7. Overall sway index on the left leg.
  8. Overall sway index on the right leg.
Under three conditions (Condition 0, condition 1 an Condition 3) at least 48 hours apart.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Dynamic balance
Time Frame: Under three conditions (Condition 0, condition 1 an Condition 3) at least 48 hours apart
For Dynamic balance Y Balance test was used. Three attempts each leg were conducted, to anterior, poster-omedial and posterolateral directions. The mean of all three reaches were analysed. Participants were instructed to stand barefoot, maintain a single-leg stance and extend the contralateral leg to reach as far as possible along specified lines. The supporting leg could not move, hands were placed on the hips. Y Balance test's score was calculated using this formula: Normalized Reach Distance = (Sum of reach distances in three directions: Limb length) × 100.
Under three conditions (Condition 0, condition 1 an Condition 3) at least 48 hours apart
Body hight
Time Frame: Befor testing
in cm
Befor testing
Body weight
Time Frame: Before testing
in kg
Before testing

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 15, 2025

Primary Completion (Actual)

April 1, 2025

Study Completion (Actual)

April 1, 2025

Study Registration Dates

First Submitted

January 6, 2026

First Submitted That Met QC Criteria

January 6, 2026

First Posted (Estimated)

January 14, 2026

Study Record Updates

Last Update Posted (Actual)

January 15, 2026

Last Update Submitted That Met QC Criteria

January 14, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Lithuanian Sports University28

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

There are no plans to share individual participant data, as the consent obtained from participants does not include permission for data sharing with other researchers.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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Clinical Trials on Condition - no exercise before testing

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