Effects of Pilates and Neuromuscular Exercises on Postural Control in Dynamic Knee Valgus
DKV-EX
Comparative Effects of Pilates and Neuromuscular Exercises on Postural Control in Dynamic Knee Valgus
1 other identifier
interventional
36
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 20, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2024
CompletedFirst Submitted
Initial submission to the registry
September 3, 2025
CompletedFirst Posted
Study publicly available on registry
September 25, 2025
CompletedSeptember 25, 2025
September 1, 2025
3 months
September 3, 2025
September 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Frontal Plane Projection Angle (FPPA)
Participants performed a single-leg vertical drop jump from a 20 cm platform with the dominant leg while keeping their hands on the waist. Knee valgus angle at landing was recorded using 2D video analysis with a camera placed 3 m in front at a height of 45 cm.
At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6)
Secondary Outcomes (2)
Isometric Strength of Gluteus Medius
At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6)
Isometric Strength of Rectus Femoris
At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6)
Other Outcomes (7)
Postural Stability Test - Overall Stability Index (Biodex)
At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6)
Postural Stability Test - Anterior-Posterior Stability Index (Biodex)
At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6)
Postural Stability Test - Medial-Lateral Stability Index (Biodex)
At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6)
- +4 more other outcomes
Study Arms (3)
Pilates Exercise Group
EXPERIMENTALParticipants 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.
Neuromuscular Exercise Group
EXPERIMENTALParticipants 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.
Control Group
NO INTERVENTIONParticipants 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.
Interventions
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.
A 6-week supervised neuromuscular training program, 18 sessions . Training emphasized balance, proprioception, dynamic stability, and strengthening of lower extremity muscles.
Eligibility Criteria
You may qualify if:
- 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)
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Şebnem Nur Alkanlead
Study Sites (1)
Atlas University
Istanbul, Kagıthane, 34403, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- 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.
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Assistant Professor of Physiotherapy, Atlas University
Study Record Dates
First Submitted
September 3, 2025
First Posted
September 25, 2025
Study Start
June 1, 2024
Primary Completion
August 20, 2024
Study Completion
August 30, 2024
Last Updated
September 25, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share