NCT07192796

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 20, 2024

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2024

Completed
1 year until next milestone

First Submitted

Initial submission to the registry

September 3, 2025

Completed
22 days until next milestone

First Posted

Study publicly available on registry

September 25, 2025

Completed
Last Updated

September 25, 2025

Status Verified

September 1, 2025

Enrollment Period

3 months

First QC Date

September 3, 2025

Last Update Submit

September 17, 2025

Conditions

Keywords

Dynamic knee valgusNeuromuscular exercisePilatesFrontal plane projection anglePostural control

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

EXPERIMENTAL

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.

Behavioral: Pilates Exercise Program

Neuromuscular Exercise Group

EXPERIMENTAL

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.

Behavioral: Neuromuscular Exercise Program

Control Group

NO INTERVENTION

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.

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.

Pilates Exercise Group

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

Neuromuscular Exercise Group

Eligibility Criteria

Age18 Years - 24 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Study Sites (1)

Atlas University

Istanbul, Kagıthane, 34403, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Knee Injuries

Condition Hierarchy (Ancestors)

Leg InjuriesWounds and Injuries

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
Model Details: 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).
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

Locations