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N/A Completed N=34 Randomized Triple-blind Prevention

Optimizing Movement After Anterior Cruciate Ligament Injury

Anterior Cruciate Ligament Injuries · Knee Osteoarthritis
Source: ClinicalTrials.gov NCT05363683 ↗
Enrolled (actual)
34
Serious AEs
0.0%
Results posted
Dec 2025
Primary outcomePrimary: Knee Flexion Moment Impulse — 0.54; 0.50 Ratio — p=0.293

Summary

Fifty percent of teenagers and young adults who suffer an anterior cruciate ligament (ACL) injury develop knee osteoarthritis (OA) within 15 years. The resulting pain, reduced quality-of-life, and increased risk for co-morbidity lead to substantial healthcare costs, inability to fulfill work and personal responsibilities, and reduced long-term health. Degeneration in articular cartilage, connective tissue that covers the ends of bones in the knee, is the hallmark of early OA development after knee injury. This deterioration can be measured by an imaging biomarker for OA development on quantitative magnetic resonance imaging (MRI). Harmful increases in MRI markers of the knee's articular cartilage occur within months of ACL injury and indicate preventative interventions should begin soon after injury. However, evidence-based interventions to prevent OA do not exist. This project will challenge the traditional OA paradigm that too much joint loading (e.g. "wear and tear") causes cartilage breakdown. A multi-disciplinary team has developed a novel visual biofeedback paradigm using portable force plates that can increase knee loading during squats within a single session after ACL reconstruction (ACLR). This study will determine the efficacy of the visual biofeedback program initiated two weeks after ACLR by assessing movement biomechanics and MRI changes in cartilage after six months later. Successful completion of this project will establish the first rehabilitation intervention to effectively and optimally load the knee joint early after ACLR, providing the initial steps to prevent OA after ACL injury.

Outcome Measures

OutcomeResultp-value
PRIMARY
Knee Flexion Moment Impulse
0.66; 0.54 0.114
PRIMARY
Cartilage T2 Relaxation Time
6.63; 5.86
SECONDARY
Knee Flexion Moment Impulse
0.66; 0.54 0.114
SECONDARY
Vertical Ground Reaction Force Impulse
0.95; 0.86 0.021 sig
SECONDARY
Peak Knee Flexion Moment
0.7; 0.7 0.867
SECONDARY
Quadriceps Strength
0.8; 0.6 0.379

Eligibility Criteria

Inclusion Criteria

  • Acute anterior cruciate ligament (ACL) injury in the past 6 months
  • ACL reconstruction in the past month or have a planned ACL reconstruction

Exclusion Criteria

  • Previous knee injury or surgery (contralateral knee)
  • Body mass index (BMI) over 35 kg/m2
  • Concomitant posterior cruciate ligament reconstruction or cartilage procedure that includes extended weight bearing restrictions and/or changes to cartilage structure
  • Current or planned pregnancy during study duratuiom
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05363683). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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