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AI-Based Video Assessment of Anterior Knee Laxity (AI-LAX)

17 september 2026 bijgewerkt door: Jacopo Conteduca, ASL Lecce

Artificial Intelligence-Based Video Assessment of Anterior Knee Laxity Compared With Rolimeter in Patients With Anterior Cruciate Ligament Injury: A Prospective Validation Study

This prospective observational validation study aims to evaluate the accuracy and reliability of artificial intelligence-based video analysis for quantifying anterior knee laxity. Participants with unilateral anterior cruciate ligament (ACL) injury and ACL-intact controls will undergo bilateral knee examination using a Rolimeter by two independent orthopedic surgeons. Three consecutive measurements will be obtained for each knee and examiner. Each examination maneuver will be video recorded using a standardized acquisition protocol including a metric reference of known dimensions.

The videos will subsequently be analyzed independently by a multimodal artificial intelligence system blinded to clinical diagnosis, MRI findings, injured side, examiner measurements, and contralateral knee measurements. AI-derived anterior tibial translation and side-to-side difference will be compared with Rolimeter measurements. The primary objective is to assess agreement between AI-derived and Rolimeter-derived side-to-side difference. Secondary objectives include inter-examiner reliability, AI repeatability and the diagnostic accuracy of AI-derived measurements for identifying ACL injury.

Studie Overzicht

Toestand

Nog niet aan het werven

Conditie

Gedetailleerde beschrijving

Each examiner will perform three consecutive Rolimeter measurements on both knees. Individual maneuvers will be video recorded so that the Rolimeter and AI measurements refer to the same mechanical examination. Videos will be pseudonymized and analyzed independently. The AI system will have no access to participant group allocation, MRI findings, injured side, Rolimeter measurements, or results from other videos belonging to the same participant.

A standardized metric reference positioned in the plane of the examined knee will be visible in each recording to permit estimation of displacement in millimeters. AI measurements will not be used for clinical decision-making.

Studietype

Observationeel

Inschrijving (Geschat)

70

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

  • Italië
      • Lecce, Italië, 73100
        • Ospedale Vito Fazzi
        • Contact:

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

16 jaar tot 55 jaar (Kind, Volwassen)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Allemaal

Bemonsteringsmethode

Niet-waarschijnlijkheidssteekproef

Studie Bevolking

Adults undergoing prospective bilateral assessment of anterior knee laxity at a single orthopedic center. The study population will include two cohorts: participants with a unilateral, complete anterior cruciate ligament (ACL) injury confirmed by magnetic resonance imaging and ACL-intact control participants without clinical evidence or history of ACL injury.

All participants will undergo the same standardized bilateral knee examination using an arthrometer performed independently by two orthopedic examiners. Each examination maneuver will be video recorded for subsequent blinded AI-based assessment of anterior tibial translation.

Beschrijving

Inclusion Criteria:

  • General inclusion criteria
  • Age ≥16 years.
  • Ability to understand the study procedures and provide written informed consent.
  • Ability to undergo bilateral clinical assessment of anterior knee laxity.

ACL-Deficient Group

  • Unilateral complete anterior cruciate ligament (ACL) injury confirmed by magnetic resonance imaging (MRI).
  • Clinical evidence of anterior knee instability compatible with ACL deficiency.
  • Contralateral knee without known ACL injury or previous ACL reconstruction.
  • ACL-Intact Control Group
  • No history of ACL injury or ACL reconstruction in either knee.
  • No clinical evidence of anterior knee instability.
  • Negative clinical assessment for ACL deficiency in both knees.

Exclusion Criteria

  • Previous ACL reconstruction or other major ligament reconstruction of either knee.
  • Bilateral ACL injury.
  • Revision ACL injury or previous ACL surgery.
  • Concomitant complete injury of another major knee ligament requiring surgical treatment.
  • Previous major knee surgery that could affect anterior tibial translation.
  • Moderate-to-severe knee osteoarthritis or radiographic osteoarthritis greater than Kellgren-Lawrence grade 1.
  • Acute fracture involving the examined lower limb.
  • Neurological, neuromuscular, or other conditions that could interfere with standardized knee examination.
  • Inability to tolerate or complete the standardized arthrometer examination.
  • Inability or unwillingness to provide informed consent or consent for study video recording.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Observatiemodellen: COHORT
  • Tijdsperspectieven: PROSPECTIVE

Cohorten en interventies

Groep / Cohort
ACL-deficient participants

Adults with a unilateral, complete anterior cruciate ligament (ACL) injury confirmed by magnetic resonance imaging (MRI). Participants will undergo bilateral anterior knee laxity assessment using a Rolimeter by two independent orthopedic examiners. Three consecutive measurements will be obtained for each knee and examiner, and each examination maneuver will be video recorded for subsequent blinded AI-based analysis. The contralateral knee will serve as the within-subject reference for calculation of the side-to-side difference.
ACL-Intact Control Group

Adults without a history or clinical evidence of ACL injury or knee instability. Participants will undergo the same standardized bilateral anterior knee laxity assessment performed by two independent orthopedic examiners using a Rolimeter, with three consecutive measurements for each knee and examiner. Each examination maneuver will be video recorded and subsequently analyzed by the AI system using the same protocol applied to the ACL-deficient cohort.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Agreement Between AI-Derived and Arthrometer-Derived Side-to-Side Difference in Anterior Tibial Translation
Tijdsspanne: Day 1 (index study examination)

Agreement between the side-to-side difference (SSD, mm) in anterior tibial translation estimated by artificial intelligence from standardized knee examination videos and the corresponding SSD obtained with an arthrometer. Agreement will be assessed using intraclass correlation coefficient (ICC, absolute agreement) and Bland-Altman analysis, including mean bias and 95% limits of agreement.
Day 1 (index study examination)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Measurement Error of AI-Derived Anterior Tibial Translation Compared With Arthrometer Measurements
Tijdsspanne: Day 1 (index study examination)

The difference between AI-derived and arthrometer-derived measurements of anterior tibial translation will be quantified in millimeters using mean absolute error (MAE), root mean square error (RMSE), mean bias, and 95% limits of agreement.
Day 1 (index study examination)
Inter-Examiner Reliability of Arthrometer Measurements
Tijdsspanne: Day 1 (index study examination)

Reliability of anterior tibial translation and side-to-side difference measurements obtained independently by two orthopedic examiners using an arthrometer. Inter-examiner reliability will be assessed using intraclass correlation coefficients with 95% confidence intervals and Bland-Altman analysis.
Day 1 (index study examination)
Agreement Between AI Measurements Derived From Examinations Performed by Different Examiners
Tijdsspanne: Day 1 (index study examination)

Agreement between AI-derived anterior tibial translation and side-to-side difference obtained from videos of knee examinations performed independently by the two examiners. This outcome will assess the robustness of AI-derived measurements with respect to examiner-related variability.
Day 1 (index study examination)
Diagnostic Accuracy of AI-Derived Side-to-Side Difference for ACL Injury
Tijdsspanne: Day 1 (index study examination)

The ability of AI-derived side-to-side difference to discriminate participants with complete anterior cruciate ligament injury from ACL-intact controls will be assessed using receiver operating characteristic (ROC) curve analysis. Area under the curve (AUC), sensitivity, specificity, positive predictive value, and negative predictive value will be calculated.
Day 1 (index study examination)
diagnostic Accuracy of Arthrometer-Derived Side-to-Side Difference for ACL Injury
Tijdsspanne: Day 1 (index study examination)

The diagnostic performance of arthrometer-derived side-to-side difference for identifying complete anterior cruciate ligament injury will be evaluated using ROC curve analysis, including AUC, sensitivity, specificity, positive predictive value, and negative predictive value.
Day 1 (index study examination)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

ASL Lecce

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

15 september 2026

Primaire voltooiing (Geschat)

31 december 2026

Studie voltooiing (Geschat)

31 december 2026

Studieregistratiedata

Eerst ingediend

12 september 2026

Eerst ingediend dat voldeed aan de QC-criteria

17 september 2026

Eerst geplaatst (Werkelijk)

22 september 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

22 september 2026

Laatste update ingediend die voldeed aan QC-criteria

17 september 2026

Laatst geverifieerd

1 september 2026

Meer informatie

Termen gerelateerd aan deze studie

Trefwoorden

Andere studie-ID-nummers

  • ASLLECCE-AILAX-2026-01

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

De-identified data may be made available from the corresponding author upon reasonable request, subject to institutional and ethical approval.

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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