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Recruiting NCT07058467

NCT07058467 Anterior Cruciate Ligaments: Studying Updates in neuroCognition After Knee Manipulation

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Clinical Trial Summary
NCT ID NCT07058467
Status Recruiting
Phase
Sponsor University of North Carolina, Chapel Hill
Condition Anterior Cruciate Ligament (ACL) Tear
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2025-08-01
Primary Completion 2026-05-31

Trial Parameters

Condition Anterior Cruciate Ligament (ACL) Tear
Sponsor University of North Carolina, Chapel Hill
Study Type INTERVENTIONAL
Phase N/A
Enrollment 30
Sex ALL
Min Age 18 Years
Max Age 35 Years
Start Date 2025-08-01
Completion 2026-05-31
Interventions
Joint Manipulation

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Brief Summary

This study will investigate whether knee joint manipulation can improve neurocognitive and neuromuscular performance in individuals with a history of anterior cruciate ligament reconstruction (ACLR). Recruitment will consist of 30 participants aged 18-35 who are 4 months to 5 years post-ACLR and demonstrate measurable reaction time delays. Using a within-subject pre-post design, participants will complete a battery of neurocognitive and neuromuscular assessments, including visuomotor reaction time and dual-task hop testing, before and after knee joint manipulation(s). The main questions the investigators aim to address are: Aim 1: Evaluate the feasibility, acceptability, and applicability of integrating knee joint manipulation into post-ACLR rehabilitation using the Implementation and Outcomes Framework. Aim 2: Determine preliminary efficacy of knee joint manipulation on neurocognitive performance in individuals with ACLR.

Eligibility Criteria

Inclusion Criteria: * Provided informed consent prior to any study procedures that are performed. * Are between the ages of 18 and 35. * Have undergone ACLR surgery. All autograft and allograft types are accepted. * Are 4-months to 10-years post-ACLR. * Injured knee playing or training for sports (recreational or organized) or during physical activity. * Have been cleared by a physician to return to activities and/or participate in this study. * Are at least the minimally clinical important difference (MCID) above the normative reaction time average for our methods as established by previous literature in at least 1 reaction time task. Exclusion Criteria: * History of concussion in the past 3 months. * The participant is pregnant. * Have a neurological disorder, including epilepsy. * Currently injured or have injured their lower extremity in the past 3 months. * Had surgery on multiple ligaments when their ACL was injured.

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