Effects of Pilates and Neuromuscular Exercises on Postural Control in Dynamic Knee Valgus

NCT ID: NCT07192796

Last Updated: 2025-09-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-01

Study Completion Date

2024-08-30

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Dynamic Knee Valgus Knee Injuries Postural Control Deficit

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants were randomized into three parallel groups: a Pilates exercise group, a neuromuscular exercise group, and a control group. Interventions were delivered over 6 weeks (18 sessions).
Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors
Single-blind design: Both participants and the outcome assessor were blinded to group allocation. Exercise providers were not blinded due to the nature of the intervention.

Study Groups

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Pilates Exercise Group

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.

Group Type EXPERIMENTAL

Pilates Exercise Program

Intervention Type BEHAVIORAL

A 6-week supervised Pilates exercise program, with 18 sessions. Exercises focused on core stabilization, posture, and lower limb alignment using mat-based and resistance band movements.

Neuromuscular Exercise Group

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.

Group Type EXPERIMENTAL

Neuromuscular Exercise Program

Intervention Type BEHAVIORAL

A 6-week supervised neuromuscular training program, 18 sessions . Training emphasized balance, proprioception, dynamic stability, and strengthening of lower extremity muscles.

Control Group

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.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Pilates Exercise Program

A 6-week supervised Pilates exercise program, with 18 sessions. Exercises focused on core stabilization, posture, and lower limb alignment using mat-based and resistance band movements.

Intervention Type BEHAVIORAL

Neuromuscular Exercise Program

A 6-week supervised neuromuscular training program, 18 sessions . Training emphasized balance, proprioception, dynamic stability, and strengthening of lower extremity muscles.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

24 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Şebnem Nur Alkan

OTHER

Sponsor Role lead

Responsible Party

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Şebnem Nur Alkan

Assistant Professor of Physiotherapy, Atlas University

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Atlas University

Istanbul, Kagıthane, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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E-22686390-050.99-41964

Identifier Type: -

Identifier Source: org_study_id

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