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Michigan Split-belt Treadmill Training Program to Improve Long-Term Knee Biomechanics After ACL Reconstruction
Mi-SPA: Michigan Split-belt Adaptation Paradigm to Improve Knee Loading After Anterior Cruciate Ligament Reconstruction (Aim 3)
Who can join
Ages 14 to 45 · All sexes
Full eligibility criteria
Inclusion Criteria: * aged 14-45 years * suffered an acute, complete ACL rupture as confirmed by MRI and physical exam * have undergone ACL reconstruction w autograft within the past 10 months * willingness to participate in testing and follow-up as outlined in the protocol * English-speaking Exclusion Criteria: * inability to provide written informed consent * female subjects who are pregnant or are planning to become pregnant (self-reported) * previous ACL injury * previous surgery to either knee * bony fracture accompanying ACL injury * patients who experienced a knee dislocation * patients who had their ACL reconstructed with an allograft * patients who underwent a multi-ligamentous and/or staged ACL reconstruction
About the study
The goal of this study is to gather pilot data to help inform a future clinical trial. As such, the investigators will employ a randomized clinical trial design, but data will only be collected on 9 total subjects. Nine subjects will be randomized to 2 split-belt intervention groups (one group where early stance loading is trained and the other where midstance loading is trained) and a placebo group.
The goal of this study is to explore the adaptations in knee loading from a 6-week split-belt training intervention.
The investigators' main question for this aim is:
1. Does knee loading, measured by the sagittal plane knee moment, change to a greater extent in the split-belt treadmill training groups compared to the placebo group? 2. Are there differences in training-related knee loading changes between individuals trained in the early stance vs. midstance loading split-belt training?
What is being tested
- Placebo Split-Belt Training (behavioral)
- Split-Belt Training (behavioral)
Sponsor: University of Michigan · Participants: 9 · Started: Aug 13, 2025
Contact the study team
- Alexa Johnson, PhD · Phone: 734-615-1297
- Riann M Palmieri-Smith, PhD, ATC · Phone: 734-615-3154
Official record on ClinicalTrials.gov — NCT06529692
Locations in the U.S.
| Michigan | University of Michigan, Ann Arbor |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.