- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06743074
Effectiveness of Different Exercise Programmes in Individuals With Dynamic Knee Valgus
August 11, 2025 updated by: hazal genc
Dynamic knee valgus (DDV) is an erroneous movement pattern of the lower limb that occurs in multiple planes.
It results from a combination of hip joint adduction, femoral anteversion, knee abduction and external tibial torsion .
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Dynamic knee valgus (DDV) is an erroneous movement pattern of the lower limb that occurs in multiple planes.
It results from a combination of hip joint adduction, femoral anteversion, knee abduction and external tibial torsion .
DDV is also referred to as a mechanism in which the knee joint moves medially relative to the hip and foot with the centre fixed to the ground.
Study Type
Interventional
Enrollment (Actual)
38
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
-
-
None Selected
-
Istanbul, None Selected, Turkey, 34353
- bahcesehır 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
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion criteria:
- Age between 18-50 years.
- Absence of any lower extremity pain.
- Having a frontal plane projection angle of 10 and above in the descent phase of squatting on one leg.
- Having active or regular physical activity.
- Volunteering to participate in the study.
Exclusion criteria:
- Active knee pain.
- History of patellar instability.
- Presence of rheumatic diseases such as osteoarthritis, rheumatoid arthritis.
- History of trauma or injury causing ligament laxity in the ankle, hip or knee.
- Having a neurological disease that may impair the ability to perform any lower limb movement.
- Having undergone any lower extremity surgery before.
- Having received physiotherapy from hip, knee and ankle in the last 6 months.
- To be benefiting from another treatment during the study.
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: foot Exercise
foot exercise
|
foot exercise
|
|
Experimental: hip exercise
|
hip exercise
|
|
Other: control group
other
|
control
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Frontal Plane Projection Angle (FPPA)
Time Frame: 6 weeks
|
FPPA is measured as the angle between a line drawn from the marked point on the proximal thigh to the knee joint and another line extending from the knee joint to the ankle during maximum knee flexion.
A 2D analysis is performed through single-leg squat (SLS), vertical jump (VJ), and single-leg landing (SLL).
An increase of 10° or more in FPPA during a single-leg squat is categorized as "Observable Dynamic Knee Valgus (DKV)."
|
6 weeks
|
|
Lower Extremity Clinical Measurements
Time Frame: 6 weeks
|
Clinical measurements help assess the functional performance of the lower extremities and prevent injuries.
Key parameters include Q-angle, hip anteversion angle, tibial torsion, ankle dorsiflexion, and rearfoot angle.
Standardized tests such as goniometer-based Q-angle measurement, Craig's test for hip anteversion, and subtalar joint neutral positioning for dorsiflexion are utilized.
|
6 weeks
|
|
Balance Evaluation
Time Frame: 6 weeks
|
Static balance was assessed with the Single Leg Stance Test (SLST), while dynamic balance was evaluated using the Y Balance Test (YBT) in three directions: anterior, posteromedial, and posterolateral.
|
6 weeks
|
|
Proprioception Assessment
Time Frame: 6 weeks
|
Proprioception was evaluated using the Active Joint Position Sense (AJPS) test, which measures the ability to replicate a target angle.
Measurements were conducted with a Baseline digital goniometer, and angular deviation was recorded to determine accuracy.
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: aleyna zeynep karcıoğlu, Bahcesehir university
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)
November 11, 2024
Primary Completion (Actual)
December 30, 2024
Study Completion (Actual)
April 3, 2025
Study Registration Dates
First Submitted
December 16, 2024
First Submitted That Met QC Criteria
December 16, 2024
First Posted (Actual)
December 19, 2024
Study Record Updates
Last Update Posted (Actual)
August 12, 2025
Last Update Submitted That Met QC Criteria
August 11, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
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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