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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05363683
Other study ID # 0652-21-FB
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 11, 2021
Est. completion date December 2024

Study information

Verified date June 2024
Source University of Nebraska
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will evaluate if a visual biofeedback program leads to improved knee outcomes after anterior cruciate ligament reconstruction. Outcome measures will include biomechanical movement patterns and markers of knee osteoarthritis on magnetic resonance imaging.


Description:

Fifty percent of teenagers and young adults who suffer an anterior cruciate ligament (ACL) injury develop radiographic 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. Articular cartilage degeneration is the hallmark sign of early OA development after knee injury. This deterioration can be measured by increased T2 and T1rho relaxation time on quantitative magnetic resonance imaging (MRI), an imaging biomarker for OA development. 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. The investigators have shown that after ACL reconstruction (ACLR), patients exhibit asymmetric movement patterns characterized by up to 62% lower knee joint loading during walking and squatting in the injured limb at two months after ACLR. These knee joint loading patterns remain 40% lower at six months. Emerging evidence suggests knee joint unloading patterns after ACL injury may increase the risk for OA development. Currently, no studies have examined the efficacy of movement-focused interventions during the first months after ACLR, which explains the lack of evidence-based interventions that successfully increase knee loading early after ACLR. This gap presents a barrier to the research team's long-term goal of preventing OA in young, active individuals before irreversible knee degeneration occurs. This project will challenge the traditional OA paradigm that too much joint loading (e.g. "wear and tear") causes cartilage breakdown. The multi-disciplinary team spanning rehabilitation, orthopaedics, radiology and biomechanics has developed a novel visual biofeedback paradigm using portable force plates that can increase knee loading during squats within a single session after ACLR. This data suggest movement is modifiable using visual feedback, but its efficacy beyond a single training session is unknown. 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 microstructure 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 in the team's work to prevent OA after ACL injury.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 34
Est. completion date December 2024
Est. primary completion date June 5, 2024
Accepts healthy volunteers No
Gender All
Age group 13 Years to 35 Years
Eligibility Inclusion Criteria: - acute ACL injury in the past 6 months - have had ACL reconstruction in the past month or have a planned ACL reconstruction Exclusion Criteria: - previous knee injury or surgery (contralateral knee) - body mass index over 35 kg/m2 - concomitant posterior cruciate ligament reconstruction or cartilage procedure that include extended weightbearing restrictions and/or changes to cartilage structure - current pregnancy - planned pregnancy during study duration

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Squat Biofeedback
The intervention group will complete bilateral squats with each limb on a separate portable force plate. They will receive real-time visual feedback on a 32-inch screen during all squats. Biofeedback conditions will be progressed from simplest (ground reaction force only) to most complex (ground reaction force plus center of pressure). This intervention will be included in additional to standard care post-operative physical therapy.
Standard Care
Standard care post-operative physical therapy

Locations

Country Name City State
United States University of Nebraska Medical Center Omaha Nebraska

Sponsors (1)

Lead Sponsor Collaborator
University of Nebraska

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Knee flexion moment impulse Between-limb ratio of knee flexion moment impulse during descent and ascent phase of bilateral squat Immediately after the intervention
Primary Cartilage T2 relaxation time Percent change in cartilage T2 relaxation time from 2 weeks to 6 months after ACL reconstruction 6 months after ACL reconstruction
Secondary Knee flexion moment impulse Between-limb ratio of knee flexion moment impulse during descent and ascent phase of bilateral squat 6 months after ACL reconstruction
Secondary Peak knee flexion moment Between-limb ratio of peak flexion moment during gait Immediately after the intervention
Secondary Peak knee flexion moment Between-limb ratio of peak flexion moment during gait 6 months after ACL reconstruction
Secondary Quadriceps strength Between-limb ratio of isometric and isokinetic quadriceps strength Immediately after the intervention
Secondary Quadriceps strength Between-limb ratio of isometric and isokinetic quadriceps strength 6 months after ACL reconstruction
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