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Patellar TendinopathyNCT07463560

Bilateral Lower Limb Biomechanics During Side-Cutting in Unilateral Patellar Tendinopathy

An observational study of Patellar Tendinopathy, run by Peking University Third Hospital at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Patellar tendinopathy (PT) is a common overuse injury in sports that involve jumping and directional changes. The biomechanical differences between individuals with PT and healthy controls during side-cutting, as well as whether both legs are similarly affected, remain unclear. Read more about this study

Who is it for?
Ages 18 to 50 yearsHealthy volunteers can take part
Conditions the study is for
Patellar Tendinopathy
How many people
60 participants
Where
1 siteChina
Study dates
15 Jul 2023to 31 May 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 50 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: Patients with PT were recruited from the outpatient clinic of Peking University Third Hospital and via hospital posters, whereas healthy controls were recruited through posters targeting healthy individuals. All participants read and signed the approved informed consent form before data collection.

Who may be able to join

  • Age 18-40 years and regular participation in sports, defined as engaging in physical activities for at least 90 minutes per week over the past three months, such as basketball, soccer, tennis, volleyball, long-distance running, and other sports activities,
  • Structural tendon changes on imaging, including tendon thickening, hypoechogenicity, and/or increased neovascularization on Doppler ultrasound, or increased signal intensity on T2-weighted Magnetic Resonance Imaging (MRI) sequences relative to normal tendon tissue, with observable localized edema, inflammation, or degenerative changes,
  • positive tenderness response upon palpation of the patellar tendon,
  • reproduction of patellar tendon pain during resisted knee extension and/or during a standardized single-leg squat test,
  • a score of ≤ 80 on the VISA-P (Victorian Institute of Sport Assessment-Patella) questionnaire.
  • Participants were reported regular participation in sports, defined as engaging in physical activities for at least 90 minutes per week over the past three months, such as basketball, soccer, tennis, volleyball, long-distance running, and other sports activities,
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  • no history of knee injury,
  • no history of lower-limb surgery,
  • normal range of motion of the lower-limb joints (hip, knee, and ankle joints with no limitations in active or passive movements, within the normal physiological range),
  • no history of chronic joint disorders, including current or pre-existing knee pain, PT, or functional impairment
  • no evidence of patellar tendon pathology on ultrasound or MRI.

Who cannot join

  • a history of trauma to other lower limb joints,
  • a history of surgery on any lower limb joint,
  • use of analgesic medication in the past two weeks,
  • the presence of other lower limb pathologies.

Trial locations and contacts

1 site in 1 country.

China1 site
  • Beijing Key Laboratory of Research and Translation for Drugs and Medical Devices in Precision Diagnosis and Treatment of Sports

    Beijing, Beijing Municipality

Other trials in China

About this study

Official title: Comparison of Bilateral Lower Limb Biomechanics During Side-Cutting Between Patients With Unilateral Patellar Tendinopathy and Healthy Controls

Patellar tendinopathy (PT) is a common overuse injury in sports that involve jumping and directional changes. The biomechanical differences between individuals with PT and healthy controls during side-cutting, as well as whether both legs are similarly affected, remain unclear. This study aimed to compare the kinematics and kinetics of the affected leg in patients with PT, their unaffected leg, and healthy controls during side-cutting. Methods: Thirty patients with PT and thirty healthy participants performed a side-cutting task. Motion capture and force plates were used to collect data. Five peak ground reaction forces (GRFs) and the corresponding hip, knee, and ankle joint angles and moments were analyzed. Statistical comparisons were performed using t-tests with Bonferroni correction.

Read the detailed description

Patellar tendinopathy (PT) is a musculoskeletal disorder characterized by localized pain at the junction of the inferior pole of the patella and the patellar tendon insertion. It is considered an overuse injury, predominantly affecting highly active populations participating in sports that involve repetitive jumping, running, and side-cutting, such as volleyball, soccer, and basketball, where the patellar tendon repeatedly stores and releases energy. The long-term accumulation of mechanical load in these activities can lead to structural changes in the tendon. Current biomechanical research on patellar tendinopathy has primarily focused on jumping tasks. Previous studies suggest that individuals with PT tend to adopt a pain-avoidance strategy by reducing knee flexion during landing to decrease patellar tendon loading, and they also demonstrate significantly reduced knee extension moments and rates of moment development at initial contact. However, some studies have found no significant differences in knee flexion angle or extension moment compared to healthy controls, yet these individuals still exhibit increased local patellar tendon stress, indicating that patellar tendon loading may be triplanar and should not be analyzed solely in the sagittal plane, highlighting the importance of also considering the frontal and transverse planes. Notably, research using individualized finite element models has systematically quantified the effects of femoral and tibial rotations in the frontal and horizontal planes on peak principal stress in the patellar tendon, showing that rotation in the horizontal plane has a significant impact on tendon stress. Since the hip joint serves as the proximal driver of femoral horizontal rotation, hip motion in the horizontal plane warrants particular attention. However, biomechanical studies examining hip, knee, and ankle joint mechanics in the horizontal plane in individuals with PT remain scarce. The side-cutting maneuver is a complex task involving single-leg landing, change of direction, and push-off, during which the lower limb experiences multi-directional impact forces from the sagittal, frontal, and horizontal planes. Research on side-cutting has primarily focused on acute injuries, such as anterior cruciate ligament rupture, with limited attention to chronic conditions like PT. Existing evidence not only confirms that side-cutting increases patellar tendon loading but also suggests that individuals with anterior knee pain may be at greater risk of injury during side-cutting, emphasizing the need for biomechanical studies of side-cutting in PT populations. A proposed framework divides the side-cutting maneuver into three phases: the initial contact-deceleration phase, the stance pivot phase, and the push-off phase, which are defined by five peak ground reaction force events, including four horizontal and one vertical peak. Previous research indicates that multi-planar loading tasks, particularly horizontal landing phases, are more sensitive than vertical landing tasks in detecting aberrant biomechanical patterns in individuals with PT. Although ground reaction forces do not directly represent patellar tendon loading, they reflect the external horizontal and vertical loads experienced by the lower limb. Therefore, using a ground reaction force-based phase analysis framework for side-cutting is particularly valuable in examining vertical and horizontal movement strategies in individuals with PT. Based on this framework, the present study aims to assess, during side-cutting, the magnitudes of each peak ground reaction force and the corresponding three-dimensional joint angles and moments of the knee, hip, and ankle in the affected limb of individuals with PT, their unaffected limb, and healthy controls.

Keywords
patellar tendinopathy, side-cutting, biomechanical characteristics

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07463560
Study groupRoleWhat they receive
Experimental grouppatients with patellar tendinopathy
control grouphealthy individuals

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Vicon 3D gait test

    All subjects wore athletic shorts, fully exposing the waist and the area below the mid-thigh. After reflective markers were attached, participants familiarized themselves with the movement collection requirements and procedures according to the testing protocol. At the start of the formal test, participants began the approach run as soon as they heard the command "Start." They sprinted at maximal speed, accurately planting the tested leg on the second force plate, after which the contralateral leg stepped at an angle of approximately 45°. A one-minute rest interval was provided between trials, and participants were confirmed to be free of any obvious signs of fatigue or discomfort before each test. No pain was elicited throughout the testing session. Each participant completed three successful trials for each lower limb, defined as trials completed according to the experimental requirements within the prescribed time, from which complete kinematic and kinetic data were collected.

    Measured: Day 1 (single time point)

Secondary outcomes (2)
  1. Visual Analogue Scale for Pain and VISA-P Scale

    Visual Analogue Scale for Pain:The VAS scale is usually a horizontal or vertical line 10 cm long with "0" and "10" marked on both ends. "0" represents "no pain" and "10" represents "worst possible pain." VISA-P Scale:A patellar tendinopathy rating scale is a reliable indicator of severity and pain. The VISA-P scale covers three areas: symptoms, function, and mobility. It consists of eight questions with a maximum score of 100. The theoretical minimum score is 0, and higher scores indicate less severe pain.

    Measured: Day 1 (single time point)

  2. Surface electromyography signal parameters

    During the side-cutting tests in both participant groups, a Delsys wireless surface electromyography (sEMG) system was used to simultaneously monitor the EMG activity of the quadriceps, hamstrings, and gluteus medius muscles.

    Measured: Day 1 (single time point)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Mar 2026
  2. Study start15 Jul 2023
  3. Primary completion30 May 2025
  4. Study completion31 May 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Retrospective
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07463560
Sponsor's protocol ID
M20260228
Status last verified
Jul 2023
First submitted
1 Mar 2026
Last updated
11 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Patellar Tendinopathy, run by Peking University Third Hospital at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 11 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Vicon 3D gait test (time frame: Day 1 (single time point)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Mar 2026.

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