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

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

Keywords

Other Study ID Numbers

  • e-10840098

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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