The Effect of Single-leg 20-degree Squats Combined With Conventional Training on the Biomechanical Characteristics of Gait After Anterior Cruciate Ligament Reconstruction Surgery

December 19, 2025 updated by: Peking University Third Hospital
Anterior cruciate ligament (ACL) tears are one of the most common sports injuries, with an ACL injury rate as high as 20.9% in the general population . Currently, the primary treatment for ACL tears is arthroscopic reconstruction surgery to restore knee stability and function . Following ACL injury, abnormal gait biomechanical characteristics persist, even after ACL reconstruction surgery (ACLR) and evidence-based rehabilitation therapy. These abnormal gait biomechanical characteristics remain unresolved, with the lower limbs exhibiting insufficient loading and stiffness, which are associated with quadriceps muscle dysfunction. Interventions for quadriceps atrophy following ACLR should be initiated early to prevent worsening of early knee pain, swelling, and abnormal gait. Additionally, since ACL reconstruction results in different biomechanical characteristics at various stages and gait phases, it is important to adopt more targeted and precise rehabilitation measures to correct biomechanical abnormalities and improve gait function in patients.

Study Overview

Detailed Description

Research Background: The anterior cruciate ligament (ACL) is one of the important anatomical structures in the knee joint, maintaining knee stability and preventing anterior displacement of the tibia. Following ACL injury, abnormal gait biomechanical characteristics persist, even after ACL reconstruction surgery (ACLR) and evidence-based rehabilitation therapy, with abnormal gait biomechanics failing to fully recover. Quadriceps atrophy is a common cause of abnormal gait biomechanics and persists long-term postoperatively. The quadriceps are closely related to knee joint function and contribute most significantly to knee joint stability and movement control. Therefore, intervention for quadriceps atrophy following ACLR should be initiated early to prevent worsening of early knee pain, swelling, and abnormal gait. Post-ACLR rehabilitation aims to protect the graft, promote its biological remodeling, and limit the extent of muscle atrophy while facilitating muscle strength recovery. Additionally, since ACL injury and reconstruction exhibit different biomechanical characteristics at various stages and gait phases, it is essential to adopt more targeted and precise rehabilitation measures to correct biomechanical abnormalities and improve gait function. Research methods: This study plans to recruit 48 patients 12 weeks post-ACL reconstruction surgery, divided into an experimental group and a control group. The experimental group will undergo single-leg mini squat (SLMS) training in addition to conventional training, with kinematic and dynamic data collected simultaneously using a three-dimensional motion capture system and force plate system; electromyographic signals will be collected from patients during gait testing. Additionally, three-dimensional finite element modeling will be used to calculate the stress distribution and peak stress on the ACL graft during SLMS. Expected Study Outcomes: This study anticipates that after 8 weeks of SLMS training, the knee flexion angle during the stance phase of walking, knee extension torque, and activity of the medial femoral muscle during walking will increase. Additionally, the study aims to confirm that SLMS training keeps stress on the ACL graft within a safe range.

Study Type

Interventional

Enrollment (Estimated)

48

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 Contact

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:

  • Clinical diagnosis of unilateral Anterior Cruciate Ligament (ACL) rupture.
  • Aged between 18 and 45 years.
  • Scheduled for primary unilateral ACL reconstruction at our hospital.
  • Presence of quadriceps atrophy, defined as the bilateral difference in quadriceps strength is >10% of the contralateral unaffected limb.
  • The operated knee has no significant redness, swelling, pain, inflammation, or limitations in range of motion and has essentially restored basic joint mobility.
  • No or only minor (Grade I) injury to the posterior cruciate ligament, medial collateral ligament, or lateral collateral ligament.

Exclusion Criteria:

  • Severe injury (Grade II or III) to the posterior cruciate ligament, medial collateral ligament, or lateral collateral ligament in the affected knee.
  • Concomitant severe meniscal tear(s) in the affected knee.
  • History of significant prior trauma or surgery to the affected knee.
  • Presence of other knee joint diseases (e.g., osteoarthritis, tumors, rheumatoid arthritis, tuberculosis).
  • Poor subject compliance or anticipated inability to complete the entire study protocol.Subject withdrawal of informed consent.
  • Any reason the subject proposes to terminate the study or is unable to complete the trial.
  • In the investigator's judgment, continued participation would adversely affect the subject's physical condition.
  • Decision by the Ethics Review Committee to terminate the study.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: experimental group
Both groups underwent conventional training. In addition, the experimental group underwent single-leg 20° squat training. Participants were required to stand for the exercise and hold onto a stable surface with their hands, while the unaffected lower limb hip joint was extended and the knee joint flexed to 90°. Participants were then instructed to bend the affected knee to 20° and hold this position for 10 seconds. They then fully extended the knee and rested in that position for 3-4 seconds. The load form can be dumbbells.
Both groups underwent conventional training. In addition, the experimental group underwent single-leg 20° squat training. Participants were required to stand for the exercise and hold onto a stable surface with their hands, while the unaffected lower limb hip joint was extended and the knee joint flexed to 90°. Participants were then instructed to bend the affected knee to 20° and hold this position for 10 seconds. They then fully extended the knee and rested in that position for 3-4 seconds. The load form can be dumbbells.
Active Comparator: control group
In the 1-8 week rehabilitation program, the goal is to strengthen the muscle strength of the affected knee joint and gradually introduce functional movement exercises, while avoiding forceful flexion and extension of the knee. The specific rehabilitation program includes: prone leg curl exercises, quadriceps resistance band training, hamstring progressive resistance exercises, backward lunge exercises, in-place small jumps, knee joint flexion with appropriate cushioning, in-place squat jumps, landing and immediately squatting for stability, repeated 15 times, each lasting 2-3 seconds, performed 2-3 sets per week, totaling 3 sessions; Wall-supported static squat exercises, repeated 5 times, performed 2-3 sets per week, totaling 3 sessions.
In the 1-8 week rehabilitation program, the goal is to strengthen the muscle strength of the affected knee joint and gradually introduce functional movement exercises, while avoiding forceful flexion and extension of the knee. The specific rehabilitation program includes: prone leg curl exercises, quadriceps resistance band training, hamstring progressive resistance exercises, backward lunge exercises, in-place small jumps, knee joint flexion with appropriate cushioning, in-place squat jumps, landing and immediately squatting for stability, repeated 15 times, each lasting 2-3 seconds, performed 2-3 sets per week, totaling 3 sessions; Wall-supported static squat exercises, repeated 5 times, performed 2-3 sets per week, totaling 3 sessions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knee joint kinematics during walking
Time Frame: Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)
Kinematic angles (flexion, rotation, and adduction) of the knee joint in the sagittal, frontal, and horizontal planes during walking.
Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)
Knee joint kinetics during walking
Time Frame: Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)]
The moment generated at the knee joint during walking.
Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)]
Gait-Synchronized Electromyographic Signals
Time Frame: Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)]

Outcome Measure 1: Raw electromyographic (EMG) activity Raw EMG signals of the rectus femoris, vastus lateralis, vastus medialis, biceps femoris, and semitendinosus muscles during specified movements.

Outcome Measure 2: Integrated electromyographic (IEMG) activity The integrated EMG (IEMG) of the rectus femoris, vastus lateralis, vastus medialis, biceps femoris, and semitendinosus muscles during specified movements.

Outcome Measure 3: Average electromyographic (AEMG) amplitude The average EMG amplitude (AEMG) of the rectus femoris, vastus lateralis, vastus medialis, biceps femoris, and semitendinosus muscles during specified movements.

Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)]
Isokinetic muscle strength
Time Frame: Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)
Quadriceps isokinetic strength test: Isokinetic biomechanical test and trainer (CON-TREX, MJ; Germany), conducted by the same tester on a constant velocity device. Three complete movements need to be collected, with an interval of 90 seconds between each test to avoid fatigue. The quadriceps muscle was tested for isokinetic and eccentric peak torque (PT) at 60°/s.
Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)
Anterior cruciate ligament stress distribution and peak.
Time Frame: Completed through study, averaging 3 months.
  • Joint flexion, rotation and adduction angles of the knee joint in the sagittal, frontal and horizontal planes during walking and squatting at 20°.
  • measured during squatting at 12 weeks post-anterior cruciate ligament reconstruction surgery. Stress and strain distribution in the anterior cruciate ligament at a 20-degree squat angle were calculated using ANSYS.
Completed through study, averaging 3 months.
Anterior cruciate ligament stress distribution and peak.
Time Frame: "through study completion, an average of 3 month".
  • the moment generated during movement, and the tibial displacement during squats at 20°.
  • measured during squatting at 12 weeks post-anterior cruciate ligament reconstruction surgery. Stress and strain distribution in the anterior cruciate ligament at a 20-degree squat angle were calculated using ANSYS.
"through study completion, an average of 3 month".

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lysholm Knee Scoring Scale
Time Frame: Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)]
The Lysholm Knee Scoring Scale, a patient-reported outcome measure assessing knee function. Scores range from 0 to 100, where higher scores indicate a better outcome.
Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)]
International Knee Documentation Committee Subjective Knee Form
Time Frame: Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)
The International Knee Documentation Committee Subjective Knee Form, a patient-reported outcome measure assessing symptoms, function, and sports activity. Scores range from 0 to 100, where higher scores indicate a better outcome.
Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)
Thigh circumference measurement
Time Frame: Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)
The circumference of the thigh, measured at a standardized anatomical location, to assess muscle atrophy or swelling. A smaller circumference indicates a worse outcome (greater atrophy or reduced swelling).
Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)

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 (Estimated)

January 10, 2026

Primary Completion (Estimated)

April 10, 2026

Study Completion (Estimated)

April 10, 2026

Study Registration Dates

First Submitted

September 1, 2025

First Submitted That Met QC Criteria

December 19, 2025

First Posted (Actual)

December 29, 2025

Study Record Updates

Last Update Posted (Actual)

December 29, 2025

Last Update Submitted That Met QC Criteria

December 19, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • M20250156

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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