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Biomechanical Monitoring of Knee Stability and Recovery in Active Individuals Following Anterior Cruciate Ligament Reconstruction

A Model-Based Approach to Monitoring Knee Stability and Functional Recovery Following Anterior Cruciate Ligament Reconstruction Using Repeated Biomechanical Assessments in Active Individuals

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626001054303
Enrollment
40
Registered
2026-08-26
Start date
2026-09-20
Completion date
2026-09-30
Last updated
2026-08-31

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

Conditions

None listed

Brief summary

This study aims to develop a better way to monitor recovery following anterior cruciate ligament (ACL) reconstruction using objective measures of knee function and movement. Participants will complete short biomechanical assessments during rehabilitation, including strength testing, movement analysis, and functional tasks such as balance, landing, and hopping. The study will investigate how knee stability, movement quality, strength, and limb symmetry change throughout recovery and return-to-sport progression. The information collected may help clinicians better understand rehabilitation progress and identify areas where additional support may be needed. The long-term goal is to improve evidence-based monitoring and decision-making following ACL reconstruction.

Interventions

Biomechanical Assessment and Feedback for Monitoring Recovery Following Anterior Cruciate Ligament (ACL) Reconstruction. What is the model-based approach? A computer model that combines data collected from video-based movement analysis, force plate measurements, and lower-limb strength testing to estimate knee function, assess movement mechanics, and monitor recovery progression following ACL reconstruction. Why: This study evaluates the use of repeated, non-invasive biomechanical assessments t

Biomechanical Assessment and Feedback for Monitoring Recovery Following Anterior Cruciate Ligament (ACL) Reconstruction. What is the model-based approach? A computer model that combines data collected from video-based movement analysis, force plate measurements, and lower-limb strength testing to estimate knee function, assess movement mechanics, and monitor recovery progression following ACL reconstruction. Why: This study evaluates the use of repeated, non-invasive biomechanical assessments to monitor recovery following anterior cruciate ligament (ACL) reconstruction. The intervention aims to provide objective measures of knee stability, movement quality, limb symmetry, lower-limb strength, and functional performance throughout rehabilitation. Assessment results will be provided to the participant’s treating physiotherapist to support rehabilitation monitoring and return-to-play decision-making. Materials - Participants will complete biomechanical assessments using: 1. Dual-camera video capture system (iPhone frontal and lateral views) to assess movement patterns and knee joint kinematics. 2. Vernier force plate technology to measure ground reaction forces and loading characteristics during functional tasks. 3. Lower-limb strength testing equipment to assess quadriceps and hamstring strength (force frame or equivalent) 4.Reflective markers to support movement tracking and biomechanical analysis (if required) 5. Functional movement tasks appropriate to the participant’s rehabilitation stage. Procedures: 1. Participant demographics and rehabilitation information will be collected, including age, sex, height, weight, sport/activity level, injury history, surgical details, time since ACL reconstruction, and current rehabilitation stage. 2.Participants will complete an initial biomechanical assessment based on their current rehabilitation stage and physiotherapist recommendations. 3. Assessments may include: Single leg hop, single leg balance, forward and lateral hops, quadricep and hamstring strength testing. Both reconstructed and uninjured limbs will be assessed to evaluate recovery and limb symmetry. Participants will complete repeated assessments over a 12month period to monitor changes in knee stability, movement quality, strength, and functional performance. Assessment results will be analysed and summarised for feedback if deemed acceptable to the treating physiotherapist. 4. Participants will undergo repeated assessments over a 12-month period, with a minimum of one assessment every 4–6 weeks (approximately 8–12 assessments per participant). Additional assessments may be completed if requested by the treating physiotherapist or if a participant reaches a new stage of rehabilitation, provided they are clinically appropriate and the participant is available. 5. Assessment results will be analysed and summarised for feedback to the treating physiotherapist where the results are considered valid and clinically interpretable. Who Provided: Biomechanical assessments will be conducted by trained research staff experienced in motion analysis, force plate testing, and lower-limb strength assessment. The participant’s treating physiotherapist will guide progression of assessment tasks to ensure they are appropriate for the participant’s rehabilitation stage. How: 1. Individual, face-to-face assessment sessions. 2. Testing will be completed alongside the participant’s existing rehabilitation programme where possible. 3. Each assessment session will take approximately 2–5 minutes depending on the rehabilitation stage and selected tasks. 4. The assessment protocol will be adapted according to participant capability and physiotherapist recommendations. 5. Testing will not replace standard rehabilitation or clinical assessment. Location: Assessments will be completed at the participant’s rehabilitation facility or the University of Canterbury Sports Lab, Christchurch, New Zealand. Tailoring: 1. Assessment tasks will be selected according to rehabilitation stage and clinical clearance. 2. Early rehabilitation assessments will focus on balance, controlled movement, and strength. 3. Later rehabilitation assessments will progress to higher-demand activities such as jumping and hopping tasks. 4. Task difficulty will be adjusted according to participant ability and rehabilitation progression. Number and Duration of Intervention Sessions: 1. Participants will complete repeated biomechanical assessment sessions over a 12-month period. 2. Each assessment session will take approximately 2–5 minutes. 3. Participants will complete a minimum of one assessment every 4–6 weeks during rehabilitation (approximately 8–12 assessments over 12 months). Additional assessments may be completed at key rehabilitation milestones if approved by the treating physiotherapist and agreed to by the participant. Monitoring Strategies: 1. Research staff will record completed assessments and monitor participant attendance. 2. Data quality checks will be performed following each assessment. 3. Any incomplete assessments, technical issues, or deviations from the assessment protocol will be documented.

Sponsors

University of Canterbury
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
14 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

Participants will be eligible if they are active individuals aged 14 years or older who have undergone anterior cruciate ligament (ACL) reconstruction within the previous 12 months and are currently participating in rehabilitation with the intention of returning to sport or physical activity. Participants must be cleared by their treating physiotherapist to complete study assessments and provide informed consent. Participants between 14-18years will be required parental consent to participate.

Exclusion criteria

Participants will be excluded if they have additional injuries or medical conditions affecting lower-limb function, are unable to safely complete assessment tasks, or cannot provide informed consent.

Outcome results

None listed

Source: ANZCTR · Data processed: Sep 19, 2026