- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07504666
Proprioception, Motor Control and Injury Risk on Female Wrestlers
March 25, 2026 updated by: Ebrar Atak, University of Yalova
Effects of a 4-Week Neuromuscular Balance Training Program on Knee Proprioception, Functional Performance, and Landing Errors in Elite Female Wrestlers: A Randomized Controlled Trial
This study aimed to examine the effect of a 4-week neuromuscular balance-based training program on landing mechanics as reflected by the Landing Error Scoring System-Real Time (LESS-RT), together with associated changes in knee proprioception (JPS), force sense (FSET), static balance (SLST), and single-leg functional performance in elite female wrestlers.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
22
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 Locations
-
-
Yalova
-
Yalova, Yalova, Turkey (Türkiye), 77100
- Yalova University
-
-
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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
• Not having suffered a knee injury or undergone surgery within the last 6 months,
- Not having a known neurological, vestibular, or rheumatological disease,
- Committing to regular participation in planned training sessions throughout the study period.
Exclusion Criteria:
- not being a volunteer
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group
proprioceptive exercise application.
The intervention process will be planned as individualized sessions, 3 days a week, for 30 minutes each, over a period of 4 weeks, and will be conducted under the supervision of a physiotherapist.
|
|
|
No Intervention: Control group
no additional intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Landing Error Scoring System (LESS)
Time Frame: t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
The Landing Error Scoring System (LESS) is an observational assessment tool used to evaluate lower extremity biomechanics during a jump-landing task.
Participants perform a standardized jump from a platform and land while their movements are recorded and analyzed based on specific criteria.
Higher LESS scores indicate a greater number of movement errors and an increased risk of lower extremity injury, particularly anterior cruciate ligament (ACL) injury.
A commonly used cut-off score is ≥5, indicating a higher risk of lower extremity injury, particularly ACL injury.
|
t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Joint Position Sense (JPS)
Time Frame: t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
With their eyes closed, the participant is seated with their knee passively brought to a 45° flexion, held for 5 seconds, and then returned to the starting position.
The participant is then asked to actively reproduce the same angle.
Three repetitions are performed for each leg, and the average absolute angular error (degrees) is calculated.
Measurement will be done using a goniometer.
There is no universally established cut-off value; higher repositioning error values indicate impaired proprioception.
|
t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of Strength Sensation with Barometric Cuff
Time Frame: t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
This innovative method will assess force perception and motor sensitivity.
A barometric cuff (e.g., DHD-3®, Biometrics Ltd.) is placed at the tibial plateau, and the participant is asked to compress the cuff during knee extension until a target pressure value is reached.
They are then asked to repeat the same movement with their eyes closed.
The difference in approach to the target pressure (absolute error, mmHg) is analyzed as the average of 3 repetitions.
There is no standardized cut-off value; greater deviation from the target pressure reflects reduced force sense accuracy
|
t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
|
Single-Leg Hop Test Battery
Time Frame: t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
The Single Leg Hop Test Battery is a functional performance assessment used to evaluate lower extremity strength, power, and dynamic stability.
It typically includes a series of hop tests such as the single hop for distance, triple hop for distance, crossover hop, and timed hop performed on one leg.
Performance is quantified based on distance or time, and results are often expressed as a limb symmetry index to assess side-to-side differences.
A limb symmetry index (LSI) of <90% is generally considered indicative of functional asymmetry and increased injury risk.
|
t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
|
Lower Extremity Functional Scale
Time Frame: t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
The Lower Extremity Functional Scale (LEFS) is a self-reported questionnaire used to assess functional status in individuals with lower extremity conditions.
It consists of 20 items evaluating difficulty in performing daily activities, each scored on a 5-point scale.
Higher total scores indicate better functional ability and lower levels of disability.
A cut-off score of <60 points is often interpreted as the presence of significant functional limitation in the lower extremities.
|
t0: baseline t1: at 4 weeks (post-intervention, after 12 sessions)
|
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 (Actual)
June 30, 2025
Primary Completion (Actual)
September 30, 2025
Study Completion (Actual)
November 20, 2025
Study Registration Dates
First Submitted
March 18, 2026
First Submitted That Met QC Criteria
March 25, 2026
First Posted (Actual)
April 1, 2026
Study Record Updates
Last Update Posted (Actual)
April 1, 2026
Last Update Submitted That Met QC Criteria
March 25, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025/221
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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