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External Focus of Attention Posttraumatic Osteoarthritis

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04922268
Enrollment
45
Registered
2021-06-10
Start date
2022-01-01
Completion date
2024-08-31
Last updated
2024-12-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Cruciate Ligament Injuries, Anterior Cruciate Ligament Rupture, Anterior Cruciate Ligament Tear, Osteo Arthritis Knee

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.

Interventions

Participants will complete 12 sessions over a 3-week period of functional movement retraining while receiving mirror feedback. Participants will be instructed to perform each functional task in a manner that keeps their knee in line with their toes.

OTHERExternal focus of attention feedback

Participants will complete 12 sessions over a 3-week period of functional movement retraining while receiving visual feedback via laser. Participants will be instructed to perform each functional task in a manner that does causes the laser to move up and down but not side-to-side.

Sponsors

Arthritis Foundation
CollaboratorOTHER
University of North Carolina, Charlotte
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Changes from baseline in lower extremity biomechanics during walking1-week post-intervention, 4-weeks post-interventionKnee and hip angles and loads measured via 3D biomechanics
Knee cartilage health1-week post-intervention, 4-weeks post-interventionKnee cartilage thickness measured using diagnostic ultrasound imaging

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026