Comparison the Gender Effects of Knee Joint and Foot Complex Alignment During Single Leg Squat in Sedentaries

November 28, 2025 updated by: Istinye University
In this study, the investigators aimed to investigate the relationship between the dynamic valgus index and the dynamic valgus index during the landing phase of the single leg squat movement of sedentary people according to gender and to evaluate the effect of the postural alignment of the ankle and foot complex on the stability of the knee joint during the single leg squat.

Study Overview

Detailed Description

Single leg squatting is the basis of many functional activities such as walking, running, landing and balance. Single leg squat is generally preferred for lower extremity rehabilitation and assessment of dynamic hip joint control, lower extremity kinematics and lower extremity alignment. Many studies have used single leg squats for knee kinematics assessment. Excessive knee valgus, hip adduction and abduction of the knee joint during the single leg squat pose a risk of injury to the anterior cruciate ligament, medial collateral ligament and other ligaments.

The single-leg squat test is frequently used clinically to provide a simple and convenient assessment of neuromuscular control for the lumbo-pelvic region. Misalignment of the lower limb can affect knee and hip kinematics during athletic movements, causing disorders such as anterior cruciate ligament lesions, iliotibial band syndrome and patellofemoral pain syndrome. The single leg squat test is a clinical functional test commonly used to assess clinical abnormal movement patterns of the lower limbs in terms of kinetic chain or coordinated muscle activity. This scale provides assessment of five dimensions: general impression, trunk posture, pelvis in space, hip joint movement and knee joint movement. Since the single-leg squat test tests both daily activity and lower limb balance ability during athletic tasks, it was deemed appropriate to perform it separately on both legs. It is a valid and reliable test preferred in the literature as a functional test that evaluates lower extremity and especially knee joint balance skills.

In the light of this information, the aim of this study was to investigate the relationship between the dynamic valgus index and the dynamic valgus index during the landing phase of the single leg squat movement of sedentary people according to gender and to evaluate the effect of the postural alignment of the ankle and foot complex on the stability of the knee joint during the single leg squat.

Study Type

Observational

Enrollment (Actual)

70

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

      • Gaziantep, Turkey (Türkiye), 27300
        • Gaziantep Şahinbey Ünaldı Aile Sağlığı Merkezi

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

Sampling Method

Probability Sample

Study Population

Healthy young people who can perform the single leg squat activity

Description

Inclusion Criteria:

  • To be between the ages of 18-30
  • To have the physical capacity to perform single leg squat activity
  • Voluntarily participate in the study

Exclusion Criteria:

  • Current pain in the trunk and lower extremities
  • Having a disease affecting the musculoskeletal system in the last six months
  • History of surgery involving the lumbar region and lower extremities
  • Having a neurological disease
  • Having a disease that affects balance (such as vertigo)
  • Diagnosis of a rheumatologic disease.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Men participants
Men participants between the ages of 18-30 years having an active lifestyle, able to squat without any pain or discomfort during the initial evaluation
During the single leg squat test, they will be asked to perform a squat every two seconds without bending forward or sideways while maintaining their balance with their hands crossed over their chest. While performing the movement three (3) times in a slow and controlled manner, they will be recorded with a video camera positioned at 90 degrees to their full height (approximately 3m). This recording will be evaluated in computer environment with Kineovea 0.9.5 motion analysis program and dynamic valgus index will be calculated. Q angle will be measured with a goniometer in both standing and supine position. Medial longitudinal arch height will be measured by navicular drop test. Foot posture of the participants will be evaluated with the Foot Posture Index developed by Redmond et al. (2006) to evaluate foot posture.
Women participants
Women participants between the ages of 18-30 years having an active lifestyle, able to squat without any pain or discomfort during the initial evaluation
During the single leg squat test, they will be asked to perform a squat every two seconds without bending forward or sideways while maintaining their balance with their hands crossed over their chest. While performing the movement three (3) times in a slow and controlled manner, they will be recorded with a video camera positioned at 90 degrees to their full height (approximately 3m). This recording will be evaluated in computer environment with Kineovea 0.9.5 motion analysis program and dynamic valgus index will be calculated. Q angle will be measured with a goniometer in both standing and supine position. Medial longitudinal arch height will be measured by navicular drop test. Foot posture of the participants will be evaluated with the Foot Posture Index developed by Redmond et al. (2006) to evaluate foot posture.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Dynamic Valgus Index(DVI)
Time Frame: 3 months
The mark between the participant's SIAS and the midpoint of the patella will be marked as the femur segment, and the mark between the patella and the foot will be marked as the tibia segment and video recording will be taken. Dynamic Valgus Index Measurement will be performed using Kineovea 0.9.5 motion analysis program. Knee frontal plane projection angle(KFPPA) will be measured with the computer program. The angle hip frontal plane projection angle(HFPPA) will be measured between the pelvis and the femur segment by determining the pelvis segment with the line connecting both SIAS marks. HFPPA will be subtracted from 90 degrees (90º - A) and KFPPA will be subtracted from 180 degrees (180º - B) and the DVI angle will be obtained by summing these two values.
3 months
Single leg squat test
Time Frame: 3 months
The participants' spina iliaca anterior superior (SIAS) in the frontal plane, the middle of the patella on both sides, and the middle of the ankle will be marked by sticking red colored tape. The test protocol will be explained, visually demonstrated, and three (3) repetitions will be made to try and get used to the test. A T-shape will be drawn on the floor with tape to facilitate the evaluation and they will be asked to hold their free foot behind their back while standing barefoot. They will be asked to perform a squat every two seconds without leaning forward and sideways, while maintaining their balance with their hands crossed on their chest. While performing the movement three (3) times in a slow and controlled manner, they will be recorded with a video camera positioned at 90 degrees to their full height (approximately 3m). It will be observed on the video whether the participants are positioned in the straight midline towards the single leg squat test line. If the patella
3 months
Foot posture index
Time Frame: 3 months
The participants' foot posture will be assessed using the Foot Posture Index developed by Redmond et al. (2006) to assess foot posture. It is mainly used to define the degree of supination, neutral or pronation position of the foot. All assessments are performed in a comfortable standing position with equal weight on both feet. This posture is reported to be close to the positions taken by the foot during the gait cycle. This index is composed of 6 assessment headings: palpation of the talus head, inclination above and below the lateral malleolus, calcaneal inversion/eversion assessment in the hindfoot, talonavicular alignment (concavity/convexity), medial arch height and forefoot abduction/adduction in the forefoot.
3 months
The demographic data of the participants
Time Frame: 3 months
Age, gender, dominant limb, occupational status, working positions, sports practiced, if any, and weekly physical activity duration of the individuals included in the study will be recorded before the tests. The dominant limb will be determined as the limb preferred by the individuals for kicking the ball.
3 months
Weight of the participants
Time Frame: 3 months
Weight of the participants were measured
3 months
Height of the participants
Time Frame: 3 months
Height of the participants were measured
3 months
Body Mass Index(BMI) of the participants
Time Frame: 3 months
BMI was calculated from weight and height data as kg/m^2
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pain assessment
Time Frame: 3 months

While performing the Squat Test, the participant will be asked if he/she has pain; if so, where it is located and will be asked to indicate the degree of pain with the Visual Analog Scale (VAS).

Questions to be asked:

Did you feel pain during squatting? If so, where did you feel pain? If you rate your pain on a visual scale (0 being the least and 10 being the most), how severe was the pain?

3 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Q angle
Time Frame: 3 months
The anterosuperior iliac crista, midpoint of the patella and tibial tubercle will be marked while the person is in supine position. The Q-angle will be measured with a goniometer by intersecting a line drawn from the anterosuperior iliac crista to the midpoint of the patella and the proximal extension of a line drawn from the tibial tubercle to the midpoint of the patella. Q angle measurements will be repeated 3 times for each side lying and standing and averaged
3 months
Medial Longitudinal Arc Height
Time Frame: 3 months
Medial Longitudinal Arch Height will be evaluated with the Navicular Drop Test. The height of the tubercle of the navicular bone above the ground will be recorded by marking on a white card while the participant is not transferring weight to the foot in a sitting position (A). Then, the height of the tubercle of the navicular bone above the ground will be marked while transferring equal weight to both feet in the standing upright position (B). The differences of the values taken during sitting and standing will be calculated and recorded in millimeters. Measurements will be taken for both sides and repeated 3 times and averaged
3 months
Tensor Fascia Lata Muscle Strength
Time Frame: 3 months
Strength of the tensor fascia lata muscle will be assessed using standardized manual muscle testing procedures.
3 months
Quadriceps Muscle Strength
Time Frame: 3 months
Strength of the quadriceps femoris muscle will be evaluated using manual muscle testing performed according to standardized clinical guidelines.
3 months
Hamstring Muscle Strength
Time Frame: 3 months
Hamstring muscle strength will be measured using standardized manual muscle testing techniques.
3 months
Gastrocnemius-Soleus Muscle Strength
Time Frame: 3 months
Strength of the gastrocnemius and soleus muscle group will be assessed using manual muscle testing with standardized patient positioning.
3 months
Tensor Fascia Lata Flexibility
Time Frame: 3 months
Flexibility of the tensor fascia lata muscle will be assessed using the Modified Ober Test, and the hip adduction angle will be recorded.
3 months
Hamstring Flexibility
Time Frame: 3 months
Hamstring flexibility will be evaluated using the Sit-and-Reach Test, and the maximal reach distance will be recorded.
3 months
Gastrocnemius Muscle Flexibility
Time Frame: 3 months
The participant was positioned in supine, with the hip and knee placed in full extension. The knee to be tested was stabilized with one hand, while the examiner grasped the heel with the other hand and positioned their forearm along the plantar surface of the foot. The examiner then applied force to bring the foot into dorsiflexion. If the foot could not reach the neutral position (90°), the muscle was considered shortened.
3 months

Collaborators and Investigators

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

Investigators

  • Study Director: Habibe Serap İnal, PhD, Istanbul Galata University
  • Principal Investigator: Mehmet Onur Savaş, MSc.c, Istinye University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

September 25, 2023

Primary Completion (Actual)

July 25, 2024

Study Completion (Actual)

July 25, 2024

Study Registration Dates

First Submitted

November 14, 2023

First Submitted That Met QC Criteria

November 28, 2025

First Posted (Estimated)

December 4, 2025

Study Record Updates

Last Update Posted (Estimated)

December 4, 2025

Last Update Submitted That Met QC Criteria

November 28, 2025

Last Verified

October 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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