- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07308431
The Effect of Single-leg 20-degree Squats Combined With Conventional Training on the Biomechanical Characteristics of Gait After Anterior Cruciate Ligament Reconstruction Surgery
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Hongshi Huang
- Phone Number: +8619861171626
- Email: z19861171626@163.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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.
|
|
Completed through study, averaging 3 months.
|
|
Anterior cruciate ligament stress distribution and peak.
Time Frame: "through study completion, an average of 3 month".
|
|
"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
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- M20250156
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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