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Clinical Trials/NCT04922268
NCT04922268
Completed
Not Applicable

External Focus of Attention Feedback to Mitigate Posttraumatic Osteoarthritis Risk After ACL Reconstruction

University of North Carolina, Charlotte1 site in 1 country45 target enrollmentJanuary 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anterior Cruciate Ligament Injuries
Sponsor
University of North Carolina, Charlotte
Enrollment
45
Locations
1
Primary Endpoint
Knee cartilage health
Status
Completed
Last Updated
last year

Overview

Brief Summary

Knee injuries, especially those to the ACL, are common among physically active people. These injuries are frequently treated with surgical reconstruction (ACL reconstruction; ACLR). While ACLR restores stability it does not protect against future injury, long-term pain, disability, and arthritis associated with these injuries. Our study is going to examine new ways to provide feedback about the way people move to determine if these are better at modifying movement patterns that are known risk factors of posttraumatic osteoarthritis development than current standard treatments. If you participate, you will be asked to undergo a movement analysis in a research laboratory while you perform tasks such as walking and hopping. After this initial assessment, you will be randomly allocated to one of 2 treatment groups. Each treatment group will perform 4 weeks (3x/week) of exercises to change the way people walk. Participants will then report for follow-up movement analysis testing 1- and 4-weeks after completing the intervention.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
August 31, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of North Carolina, Charlotte
Responsible Party
Principal Investigator
Principal Investigator

Abbey Thomas, PhD

Assistant Professor

University of North Carolina, Charlotte

Eligibility Criteria

Inclusion Criteria

  • history of primary, unilateral ACL reconstruction 6-24 months prior to enrollment
  • cleared to return to full activity by treating orthopedic surgeon

Exclusion Criteria

  • Body mass index \>35 kg/m2
  • History of musculoskeletal injury sustained 3 months prior to enrollment
  • Current participation in formal post-operative rehabilitation

Outcomes

Primary Outcomes

Knee cartilage health

Time Frame: 1-week post-intervention, 4-weeks post-intervention

Knee cartilage thickness measured using diagnostic ultrasound imaging

Changes from baseline in lower extremity biomechanics during walking

Time Frame: 1-week post-intervention, 4-weeks post-intervention

Knee and hip angles and loads measured via 3D biomechanics

Study Sites (1)

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