Assessing ACL injury risk in healthy athletes
Official title: Baseline ACL Injury Risk Screening and Normative Data
Run by Sanford Health · NCT06635668 · Data updated 2026-11-12
This study is trying to see how muscle strength and movement patterns in healthy athletes can help predict the risk of ACL injuries over a year.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 10 Years to 65 Years |
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | Sanford Health Academic / other |
| Locations | 1 site (Fargo, North Dakota) |
| Status | Recruiting |
| Started | July 19, 2022 |
| Main results expected | July 1, 2032 |
| Study ends | July 1, 2033 |
| Registry record updated | April 17, 2026 |
| Trial ID | NCT06635668 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are healthy athletes aged 10 to 65 participating in organized competitive sports.
✕Probably not a fit
Patients who are currently injured or pregnant will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational cohort study aims to create a database of normative biomechanics for healthy athletes while monitoring them for new musculoskeletal injuries over a year. It focuses on quantifying muscle strength, movement patterns, and biomechanics to understand their relationship with ACL injury risk. Using advanced markerless 3D motion capture technology, the study will gather high-fidelity data to develop algorithms for assessing individual injury risk. Participants will undergo an injury risk screen and complete follow-up surveys to report any new injuries.
Why it matters
Potential benefit: If successful, this study could lead to improved injury prevention strategies for athletes, particularly concerning ACL injuries.
How similar studies have gone: Other studies have shown success in using biomechanical assessments to predict injury risk, making this approach promising.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Healthy athletes participating in formal, organized, competitive sports between the ages of 10 and 65 years old
Where it's running
-
Sanford Health
Fargo, North Dakota, United States Recruiting
Study contacts
- Principal investigator: Colin Bond, PhD, MBA — Sanford Health
- Study coordinator: Colin Bond, PhD, MBA
- Email: colin.bond@sanfordhealth.org
- Phone: 701-417-6170
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Using concentrated bone marrow to improve outcomes in knee surgery
This study is testing if using concentrated bone marrow during knee surgery can help people recover better and feel less pain after having their ACL surgery redone.
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Motor imagery–enhanced rehab after ACL reconstruction
This study tests whether mentally practicing movement can improve knee function and brain activity after ACL reconstruction, in comparison with standard rehab.
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Functional Movement Training vs Functional Stability Training after ACL Surgery
This randomized trial tests whether a functional movement program or a stability-focused program helps 18-35 year old athletes recover after ACL surgery.
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Intraoperative Energy Use During ACL Surgery
This study tests how much workload a surgeon experiences during ACL reconstruction procedures while wearing a Hexoskin shirt.
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Differences in Outcomes After Allograft vs Autograft in Revision ACL Repair
This study looks at whether using donor tissue (allograft) versus the patient’s own tissue (autograft) in revision ACL surgery leads to different results.
-
Perturbation Training vs Functional Activities after ACL Reconstruction
This study tests whether perturbation training or task-oriented functional activities help people 18–45 with ACL reconstruction recover better than standard rehab.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.