- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07341555
Effect of Squats on Postural Stability, Bilateral Coordination and Dynamic Balance
IMMEDIATE EFFECTS OF SQUATS PERFORMED ON STABLE AND UNSTABLE SURFACES ON POSTURAL STABILITY, BILATERAL COMPARISON AND DYNAMIC BALANCE
Study Overview
Status
Conditions
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kauno M. Sav.
-
Kaunas, Kauno M. Sav., Lithuania, 44221
- Department of health promotion and rehabilitation
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- age between 18 and 35 years,
- voluntary consent to participate in the study.
Exclusion Criteria:
- history of lower limb injury within the past six months,
- inability to maintain postural balance during testing.
Study Plan
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.
|
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:
|
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Lithuanian Sports University28
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Healthy Subjects
-
BiogenCompletedHealthy Adult Subjects | Healthy Elderly SubjectsUnited States
-
PfizerCompletedHealthy Adult Subjects and Healthy Elderly SubjectsBelgium
-
PfizerCompletedHealthy Subjects | Healthy ParticipantsUnited States
-
National Heart, Lung, and Blood Institute (NHLBI)CompletedHealthy | Healthy Subjects | ImmunosuppressionUnited States
-
Lund UniversityCompletedHealthy Subjects | Diet, HealthySweden
-
Vichy LaboratoiresCentre de Pharmacologie Clinique Applique a la DermatologieCompletedHealthy Subjects | Healthy AdultFrance
-
Yuhan CorporationNot yet recruiting
-
Central Hospital, Nancy, FranceNot yet recruitingHealthy SubjectsFrance
-
Lutroo Imaging LLCStanford UniversityRecruiting
Clinical Trials on Condition - no exercise before testing
-
University of PennsylvaniaNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Completed
-
University Hospital, Clermont-FerrandUniversité d'Auvergne; Tza Nou - Maison médicale pour enfants et adolescentes... and other collaboratorsCompleted
-
University Hospital, Clermont-FerrandAME2P Laboratory, Clermont Auvergne UniversityCompleted
-
New York Blood CenterCompleted
-
Universidad de GranadaUniversity Hospital Virgen de las Nieves; Instituto Mixto Universitario Deporte... and other collaboratorsCompletedHealthy Aging | Blood Flow | Cognitive Function 1, Social | Cerebrovascular CirculationSpain
-
University of BergenHelse Vest; The Royal Norwegian Ministry of HealthCompleted
-
Texas Christian UniversityCompletedEndothelial DysfunctionUnited States
-
Claude Bernard UniversityCompletedStress, Psychological | Stress, Physiological | Rumination | Exam Stress | Performance AnxietyFrance
-
University Hospital PadovaNot yet recruitingEffect of Drying Before Plastic Wrapping on Thermal Losses in Very Preterm Infants at Birth (NEODRY)Temperature Regulation; Disorder, Fetus or NewbornItaly
-
Etzel ClinicUnknownShoulder Instability