The Effect of Single-leg 20-degree Squats Combined With Conventional Training on the Biomechanical Characteristics of Gait After Anterior Cruciate Ligament Reconstruction Surgery
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- What is being studied
- The protocol lists: single-leg 20° squat training, regular training.
- Who it may be relevant to
- Registry conditions: Anterior Cruciate Ligament Injuries. Basic parameters: 18 years — 45 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
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.
Interventions
- Behavioral single-leg 20° squat training
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. Th - Behavioral regular training
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, la
Primary outcome measures
- 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)]
- 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)]]
- 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)]]
- Isokinetic muscle strength [Time frame: 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.]
- Anterior cruciate ligament stress distribution and peak. [Time frame: "through study completion, an average of 3 month".]
Secondary outcome measures (3)
- 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)]]
- 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)]
- Thigh circumference measurement [Time frame: Assessed at 12 weeks post-operation and again after 8 weeks of intervention (total assessment period of 2 months)]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07308431 · M20250156