- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07406516
Identification of Kinematic Variables Specific of Patellar Tendinopathy in Athletes at Risk (TENVOL)
February 5, 2026 updated by: University Hospital, Montpellier
This research aims to identify and monitor specific kinematic markers associated with patellar tendinopathy in athletes at risk.
Using a markerless motion capture system, vertical jump tests will be analyzed to detect early biomechanical changes in the knees, hips, trunk, and ankles.
By comparing injured participants, the study seeks to improve early diagnosis and personalized prevention strategies for patellar tendinopathy.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
- Diagnostic test: The intervention consists of a series of vertical jump tests captured using high-resolution cameras with markerless motion capture technology.
- Diagnostic test: The intervention consists of a series of vertical jump tests captured using high-resolution cameras with markerless motion capture technology at 6 months and 12 months
Detailed Description
Patellar tendinopathy, also known as Jumper's knee, is the most common pathology in elite sports, with 30% of diagnoses occurring in volleyball.
Among elite volleyball players, the prevalence of this overuse-related condition ranges between 40% and 50%, resulting in anterior knee pain during daily and recreational activities, which can lead to deficits in strength and sports performance.
To date, investigator can determine whether a patient has had a history of tendinopathy through modifications in biomechanical jump-landing strategies.
However, there is a lack of early biomechanical markers to identify the onset of patellar tendinopathy and thus prevent its chronic progression.
A preventive strategy using markerless motion capture technology, providing quantitative and visual feedback of a 3D human body model, shows promise.
Investigators hypothesize that jump-landing kinematic analysis using markerless technology could identify early kinematic markers specific to patellar tendinopathy, distinguishing affected individuals from a non-tendinopathy population.
This could ultimately help identify motor strategies following the onset of patellar tendinopathy A prospective longitudinal multicenter cohort.
After signing the consent form, participants will undergo a medical examination, including a clinical assessment, a SLDS test, a Doppler ultrasound of the patellar tendon, and evaluation using the VISA-PF and OSTRC-P scores.
Following a standardized 10-minute warm-up, participants will perform vertical jump tests captured by high-resolution cameras, analyzed using markerless motion capture technology.
These assessments will be conducted at inclusion and at 3, 6, 9, and 12 months.
Additional medical visits will occur if symptoms arise outside of testing.
Study Type
Interventional
Enrollment (Estimated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Benjamin BEN ZAKI
- Phone Number: +336 66 09 13 43
- Email: b-benzaki@chu-montpellier.fr
Study Locations
-
-
-
Montpellier, France
- Sports Medicine and Traumatology LAPEYRONIE Hospital - Montpellier University Hospital
-
Contact:
- Benjamin BEN ZAKI
- Phone Number: +336 66 09 13 43
- Email: b-benzaki@chu-montpellier.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
- Subject aged between 18 and 45 years
- Male subject
- Regularly participating in physical activity involving jumping (a predisposing factor for patellar tendinopathy) twice a week for at least one year.
- Participants affiliated with or covered by a social security scheme
SPECIFIC INCLUSION CRITERIA FOR THE PATELLAR TENDINOPATHY GROUP
Patients with at least 2 of the following 3 criteria:
- Modified Öhberg score ≥2 according to L Öhberg, H Alfredson (2002)
- VISA-PF < 80/100 according to Kaux et al. (2016) and/or OSTRC P ≥ 6/100 according to Owoeye et al. (2018)
- Single Leg Decline Squat (SLDS): VAS ≥ 1/10 with pain mapping at the patellar tendon; according to Coombes et al. (2020)
SPECIFIC INCLUSION CRITERIA FOR THE HEALTHY GROUP
Patients with 0 or 1 of the following 3 criteria:
- Modified Öhberg score ≥2 according to L Öhberg, H Alfredson (2002)
- VISA-PF < 80/100 according to Kaux et al. (2016) and/or OSTRC P ≥ 6/100 according to Owoeye et al. (2018)
- Single Leg Decline Squat (SLDS): VAS ≥ 1/10 with pain mapping at the patellar tendon; according to Coombes et al. (2020)
Non inclusion Criteria:
- Significant medical and surgical history involving the lower limbs (e.g., ACL ligament reconstruction, meniscectomy, etc.)
- Contraindications to participating in sports activities
- Other pathologies involving the lower limbs (< 6 months), e.g., torn knee ligaments, ankle sprain, knee sprain, etc.
- Participants who have not given their informed consent
- Participants subject to legal protection measures (legal guardianship, conservatorship, curatorship)
- Participants deprived of their liberty by judicial or administrative decision
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: patellar tendinopathy group
Diagnostic Test: The intervention consists of a series of vertical jump tests captured using high-resolution cameras with markerless motion capture technology.
|
Participants will undergo clinical evaluations including the Single Leg Decline Squat (SLDS) test, VISA-PF, OSTRC-P questionnaires, and Doppler ultrasound of the patellar tendon.
These assessments will take place at baseline (T0) and follow-up periods (M3, M6, M9, M12) to track the evolution of kinematic markers and clinical symptoms related to patellar tendinopathy.
|
|
Other: healthy group
Diagnostic Test: The intervention consists of a series of vertical jump tests captured using high-resolution cameras with markerless motion capture technology.
|
Participants will undergo clinical evaluations including the Single Leg Decline Squat (SLDS) test, VISA-PF, OSTRC-P questionnaires, and Doppler ultrasound of the patellar tendon.
These assessments will take place at baseline (T0) and follow-up periods ( M6 et M12) to track the evolution of kinematic markers and clinical symptoms related to patellar tendinopathy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Variations of knee flexion angle at initial contact at 3 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the initial visit and the 3-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the initial visit and the 3-month visit
|
|
Variations of knee flexion angle at initial contact at 6 months
Time Frame: Between the 3-month visit and the 6-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 3-month visit and the 6-month visit
|
|
Variations of knee flexion angle at initial contact at 9 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the 6-month visit and the 9-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 6-month visit and the 9-month visit
|
|
Variations of knee flexion angle at initial contact at 12 months
Time Frame: Between the 9-month visit and the 12-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 9-month visit and the 12-month visit
|
|
Variations of the maximum knee flexion angle at 3 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the initial visit and the 3-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the initial visit and the 3-month visit
|
|
Variations of the maximum knee flexion angle at 6 months
Time Frame: Between the 3-month visit and the 6-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 3-month visit and the 6-month visit
|
|
Variations of the maximum knee flexion angle at 9 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the 6-month visit and the 9-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 6-month visit and the 9-month visit
|
|
Variations of the maximum knee flexion angle at 12 months
Time Frame: Between the 9-month visit and the 12-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 9-month visit and the 12-month visit
|
|
Variations of the range of motion (ROM) of the knee between initial contact and maximum flexion angle at 3 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the initial visit and the 3-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the initial visit and the 3-month visit
|
|
Variations of the range of motion (ROM) of the knee between initial contact and maximum flexion angle at 6 months
Time Frame: Between the 3-month visit and the 6-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 3-month visit and the 6-month visit
|
|
Variations of the range of motion (ROM) of the knee between initial contact and maximum flexion angle at 9 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the 6-month visit and the 9-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 6-month visit and the 9-month visit
|
|
Variations of the range of motion (ROM) of the knee between initial contact and maximum flexion angle at 12 months
Time Frame: Between the 9-month visit and the 12-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 9-month visit and the 12-month visit
|
|
Variations of the angle at the peak of the vertical ground reaction force (VGRF) at 3 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the initial visit and the 3-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the initial visit and the 3-month visit
|
|
Variations of the angle at the peak of the vertical ground reaction force (VGRF)at 6 months
Time Frame: Between the 3-month visit and the 6-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 3-month visit and the 6-month visit
|
|
Variations of the angle at the peak of the vertical ground reaction force (VGRF) at 9 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the 6-month visit and the 9-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 6-month visit and the 9-month visit
|
|
Variations of the angle at the peak of the vertical ground reaction force (VGRF) at 12 months
Time Frame: Between the 9-month visit and the 12-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 9-month visit and the 12-month visit
|
|
Comparison of variation between healthy group and patellar tendinopathy group of knee flexion angle at initial contact at 6 months
Time Frame: Between the two 6-month visits of the two groups
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the two 6-month visits of the two groups
|
|
Comparison between the healthy group and the patellar tendinopathy group of variation of the maximum knee flexion angle at 6 months
Time Frame: Between the two 6-month visits of the two groups
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the two 6-month visits of the two groups
|
|
Comparison between the healthy group and the patellar tendinopathy group of variations of the range of motion (ROM) of the knee between initial contact and maximum flexion angle at 6 months
Time Frame: Between the two 6-month visits of the two groups
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the two 6-month visits of the two groups
|
|
Comparison between the healthy group and the patellar tendinopathy group of variations of the angle at the peak of the vertical ground reaction force (VGRF)at 6 months
Time Frame: Between the two 6-month visits of the two groups
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the two 6-month visits of the two groups
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Variations of the angle of flexion of the trunk, hips, knees, and ankles at initial contact at 3 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the initial visit and the 3-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the initial visit and the 3-month visit
|
|
Variations of the angle of flexion of the trunk, hips, knees, and ankles at initial contact at 6 months
Time Frame: Between the 3-month visit and the 6-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 3-month visit and the 6-month visit
|
|
Variations of the angle of flexion of the trunk, hips, knees, and ankles at initial contact at 9 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the 6-month visit and the 9-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 6-month visit and the 9-month visit
|
|
Variations of the angle of flexion of the trunk, hips, knees, and ankles at initial contact at 12 months
Time Frame: Between the 9-month visit and the 12-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 9-month visit and the 12-month visit
|
|
Variations of the maximum flexion angle of the trunk, hips, knees, and ankles upon landing at 3 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the initial visit and the 3-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the initial visit and the 3-month visit
|
|
Variations of the maximum flexion angle of the trunk, hips, knees, and ankles upon landing at 6 months
Time Frame: Between the 3-month visit and the 6-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 3-month visit and the 6-month visit
|
|
Variations of the maximum flexion angle of the trunk, hips, knees, and ankles upon landing at 9 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the 6-month visit and the 9-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 6-month visit and the 9-month visit
|
|
Variations of the maximum flexion angle of the trunk, hips, knees, and ankles upon landing at 12 months
Time Frame: Between the 9-month visit and the 12-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 9-month visit and the 12-month visit
|
|
Variations of the range of motion (ROM) of the trunk, hips, knees, and ankles between initial contact and maximum flexion angle upon landing at 3 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the initial visit and the 3-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the initial visit and the 3-month visit
|
|
Variations of the range of motion (ROM) of the trunk, hips, knees, and ankles between initial contact and maximum flexion angle upon landing at 6 months
Time Frame: Between the 3-month visit and the 6-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 3-month visit and the 6-month visit
|
|
Variations of the range of motion (ROM) of the trunk, hips, knees, and ankles between initial contact and maximum flexion angle upon landing at 9 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the 6-month visit and the 9-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 6-month visit and the 9-month visit
|
|
Variations of the range of motion (ROM) of the trunk, hips, knees, and ankles between initial contact and maximum flexion angle upon landing at 12 months
Time Frame: Between the 9-month visit and the 12-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 9-month visit and the 12-month visit
|
|
Variations of the angle at the peak of the vertical ground reaction force (VGRF) of the hips, knees, and ankles upon landing at 3 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the initial visit and the 3-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the initial visit and the 3-month visit
|
|
Variations of the angle at the peak of the vertical ground reaction force (VGRF) of the hips, knees, and ankles upon landing at 6 months
Time Frame: Between the 3-month visit and the 6-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 3-month visit and the 6-month visit
|
|
Variations of the angle at the peak of the vertical ground reaction force (VGRF) of the hips, knees, and ankles upon landing at 9 months (only for patients in the patellar tendinopathy group)
Time Frame: Between the 6-month visit and the 9-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 6-month visit and the 9-month visit
|
|
Variations of the angle at the peak of the vertical ground reaction force (VGRF) of the hips, knees, and ankles upon landing at 12 months
Time Frame: Between the 9-month visit and the 12-month visit
|
The participant will perform the required vertical jump tests.
The kinematic data will be captured by the investigating physical therapist specializing in motion analysis using a camera and markerless technology.
|
Between the 9-month visit and the 12-month visit
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 1, 2026
Primary Completion (Estimated)
May 1, 2029
Study Completion (Estimated)
May 1, 2029
Study Registration Dates
First Submitted
February 5, 2026
First Submitted That Met QC Criteria
February 5, 2026
First Posted (Actual)
February 12, 2026
Study Record Updates
Last Update Posted (Actual)
February 12, 2026
Last Update Submitted That Met QC Criteria
February 5, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RECHMPL25_0117
- 2025-A01948-41 (Registry Identifier: IdRCB)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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