- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06257303
Relationship Between Knee Valgus and Landing Biomechanics
Investigation of the Correlation Between Dynamic Knee Valgus and Landing Biomechanics, Core Endurance and Ankle Dorsiflexion in Adolescent Female Basketball Players
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Pelin Pişirici, PT, PhD
- Phone Number: +905055016076
- Email: pelinpisirici@gmail.com
Study Contact Backup
- Name: Nilsu Akar, PT
- Phone Number: +905345100701
- Email: fztakarr@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Having been training basketbol for at least 6 months,
- Being between the ages of 10-19
- Being female
- Having an increase of 10 degrees or more in the frontal plane projection angle (for the valgus group)
- Having a frontal plane projection angle at normal values (for the control group)
- No active pain in the lower extremity
- No mental and psychological problems
Exclusion Criteria:
- Non-volunteer athletes
- Having a body mass index of 30 kg/m² and above
- Having undergone lower extremity surgery
- Having chronic knee instability.
- Having had a meniscus or ligament injury
- Having a cardiac, musculoskeletal, vestibular and neurological disease
- Having been using corticosteroids and nonsteroidal drugs for a long time.
- Being pregnant.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Valgus Group
If there is an increase of 10 degrees or more in the frontal plane projection angle while squatting on one leg, the participant will be included in this group.
|
During the frontal plane projection angle (FPPA) measurement, a straight line will be drawn from the anterior superior spina iliaca along the femur to the midpoint of the patella, and the midpoint of the ankle will be determined as the reference point by a straight line drawn from the midpoint of the patella.
Participants will stand with their feet aligned in the sagittal plane and their arms crossed across their chests.
By prior instruction, subjects will be asked to squat up to 60º knee flexion in a controlled manner without losing their balance, before returning to the starting position.
Digital recordings of the frontal plane will be made while individuals perform a single-leg squat test at 60º knee flexion 3 times.
The FPPA degree is measured from the medial aspect of the knee and calculated by subtracting 360.
FPPA of 195° and above will be considered pathological.
|
Active Comparator: Control Group
If the frontal plane projection angle is in the normal values while squatting on one leg, the participant will be included in this group.
|
During the frontal plane projection angle (FPPA) measurement, a straight line will be drawn from the anterior superior spina iliaca along the femur to the midpoint of the patella, and the midpoint of the ankle will be determined as the reference point by a straight line drawn from the midpoint of the patella.
Participants will stand with their feet aligned in the sagittal plane and their arms crossed across their chests.
By prior instruction, subjects will be asked to squat up to 60º knee flexion in a controlled manner without losing their balance, before returning to the starting position.
Digital recordings of the frontal plane will be made while individuals perform a single-leg squat test at 60º knee flexion 3 times.
The FPPA degree is measured from the medial aspect of the knee and calculated by subtracting 360.
FPPA of 195° and above will be considered pathological.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Landing Error Scoring System
Time Frame: Baseline
|
The Landing Error Scoring System (LESS) is a screening tool used to identify athletes who exhibit movement patterns that pose a high risk of injury in post-jump landing biomechanics.
Evaluaters will score 17 items based on movements during the jump-landing task.
The overall LESS score ranges from 0 to 17 errors, with lower scores reflecting fewer landing errors.
An error score of five or more indicates poor jumping technique and is associated with a higher risk of lower extremity injury.
Participants will begin LESS standing on a 30 cm high box and will be asked to jump forward a distance equal to half their height (indicated by a line on the ground) and make a maximum vertical jump once they land.
Participants will be provided with a verbal explanation and visual demonstration before testing and will be allowed to try the procedure until they become familiar with it.
Each participant will complete 3 trials of LESS and the resulting average will be considered for analysis.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Core endurance assessment tests
Time Frame: Baseline
|
The prone plank test will be used to evaluate trunk flexor endurance. For the prone plank test, participants will maintain a prone position in which their body weight is supported by the toes and forearms. The side plank test will be performed with the participant lying on their side, supported by their foot and elbow. The side plank test will be performed on both sides. Participants will be instructed to maintain a neutral position of the spine and pelvis and breathe normally during the test. Each test will be terminated when the participant is unable to maintain posture or their pelvis moves up or down five or more cm. Each hold time will be recorded using a stopwatch. When 1 minute is completed in both tests, chorea muscle strength will be considered sufficient. |
Baseline
|
Weight bearing lunge test
Time Frame: Baseline
|
Weight-bearing lunge test (WBLT) is frequently used in individuals with ankle instability to determine dorsiflexion normal joint movement.
During WBLT the participant puts his hands on the wall and takes one leg forward and the other leg helps balance behind.
The maximum distance that the knee touches the wall is recorded without allowing the heel of the front foot to lose contact with the ground.
The clinically significant value for WBLT was determined as 2.5 cm.
|
Baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NA-LandingB
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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