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Effects of Pilates and Neuromuscular Exercises on Postural Control in Dynamic Knee Valgus (DKV-EX)

Ş

Şebnem Nur Alkan

Status

Completed

Conditions

Knee Injuries
Postural Control Deficit
Dynamic Knee Valgus

Treatments

Behavioral: Pilates Exercise Program
Behavioral: Neuromuscular Exercise Program

Study type

Interventional

Funder types

Other

Identifiers

NCT07192796
E-22686390-050.99-41964

Details and patient eligibility

About

This randomized controlled trial aims to investigate the effects of neuromuscular and Pilates exercise programs compared with a control group in young adults with dynamic knee valgus (DKV). Thirty-six participants were randomly assigned to neuromuscular, Pilates, or control groups. The intervention groups completed a supervised exercise program three times per week for six weeks (18 sessions).

The primary outcome is the frontal plane projection angle (FPPA) during single-leg tasks. Secondary outcomes include muscle strength, balance, and vertical jump performance.

Full description

This prospective, single-blind randomized controlled trial was designed to evaluate the comparative effects of Pilates and neuromuscular exercise training on lower extremity alignment and postural control in young adults with dynamic knee valgus (DKV). Ethical approval was obtained from the Istanbul Atlas University Non-Interventional Scientific Research Ethics Committee (Approval No: E-22686390-050.99-41964, 03/05/2024).

A total of 45 participants aged 18-24 years, all right-leg dominant, were initially enrolled and randomized into three groups: Pilates, neuromuscular exercise, and control (15 in each group). Randomization was performed using computerized allocation. Due to dropouts, 36 participants (12 per group) completed the study between June and August 2024.

The interventions consisted of a 6-week supervised program (18 sessions, 3 times per week). Both Pilates and neuromuscular protocols were progressive in intensity, incorporating resistance bands, core stabilization, and functional balance exercises. The control group did not receive any intervention but underwent the same baseline and post-intervention assessments.

The primary outcome was the frontal plane projection angle (FPPA) during single-leg squat and single-leg drop jump tasks, measured using 2D video analysis.

The secondary outcomes included:

Isometric strength of the gluteus medius and rectus femoris measured with a handheld dynamometer,

Balance performance assessed separately by the Biodex Postural Stability Test (overall, anterior-posterior, and medial-lateral stability indices) and the Limits of Stability Test,

Functional performance assessed by the OptoJump system, including vertical jump height, vertical jump power, and reactive strength index.

All assessments were conducted at baseline and after 6 weeks by the same physiotherapist to ensure intra-rater reliability.

Enrollment

36 patients

Sex

All

Ages

18 to 24 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • having asymptomatic dynamic knee valgus
  • being between 18 and 24 years of age
  • having no medical history, a body mass index (BMI) between 18 and 24
  • no history of orthopedic, neurological, vascular, systemic, or rheumatic diseases
  • no complaints of pain in any part of the body during physical activities
  • the ability to communicate in Turkish (both written and verbal)

Exclusion criteria

  • individuals with hip anteversion or retroversion or other postural disorders affecting knee kinematics, those unable to perform the exercises as demonstrated, those experiencing pain during exercises (VAS >5)
  • individuals with a history of orthopedic surgery, those with strength deficits between extremities
  • the presence of cognitive or psychological disorders that could hinder cooperation
  • pregnancy or suspected pregnancy
  • sleep disorders, regular medication use, intake of painkillers, sedatives, or psychiatric drugs within the last 24 hours
  • history of chronic systemic, rheumatologic, neurological, or vascular diseases

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

36 participants in 3 patient groups

Pilates Exercise Group
Experimental group
Description:
Participants in this group completed a 6-week supervised Pilates exercise program, with 18 sessions. The program included mat-based and resistance band exercises focusing on core stabilization and postural alignment.
Treatment:
Behavioral: Pilates Exercise Program
Neuromuscular Exercise Group
Experimental group
Description:
Participants in this group performed a progressive neuromuscular training program for 6 weeks, with 18 supervised sessions. The program emphasized balance, proprioception, dynamic stability, and strengthening of lower extremity muscles.
Treatment:
Behavioral: Neuromuscular Exercise Program
Control Group
No Intervention group
Description:
Participants in this group did not receive any exercise intervention during the 6-week period. They underwent the same baseline and post-intervention assessments as the experimental groups but continued with their usual daily activities.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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