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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 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. |
|
| 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. |
|
| 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. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Pilates Exercise Program | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| 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) |
| Measure | Description | Time Frame |
|---|---|---|
| Isometric Strength of Gluteus Medius | Isometric strength of the gluteus medius muscle was measured using the PowerTrack-II handheld dynamometer in a standardized side-lying position. | At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6) |
| Isometric Strength of Rectus Femoris |
| Measure | Description | Time Frame |
|---|---|---|
| Postural Stability Test - Overall Stability Index (Biodex) | Overall stability index from the Biodex Postural Stability Test was recorded to evaluate total postural control. | At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6) |
| Postural Stability Test - Anterior-Posterior Stability Index (Biodex) |
Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Atlas University | Istanbul | Kagıthane | 34403 | Turkey (Türkiye) |
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| ID | Term |
|---|---|
| D007718 | Knee Injuries |
| ID | Term |
|---|---|
| D007869 | Leg Injuries |
| D014947 | Wounds and Injuries |
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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).
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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.
| Neuromuscular Exercise Program | Behavioral | A 6-week supervised neuromuscular training program, 18 sessions . Training emphasized balance, proprioception, dynamic stability, and strengthening of lower extremity muscles. |
|
Isometric strength of the rectus femoris muscle was measured using the PowerTrack-II handheld dynamometer in a standardized seated position with 90° knee flexion. |
| At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6) |
The anterior-posterior stability index was measured with the Biodex Postural Stability Test to assess directional balance control. |
| At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6) |
| Postural Stability Test - Medial-Lateral Stability Index (Biodex) | The medial-lateral stability index was measured with the Biodex Postural Stability Test to assess directional balance control. | At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6) |
| Limits of Stability Test (Biodex) | Limits of Stability test measured weight-shifting ability toward illuminated targets using the Biodex Balance System. | At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6) |
| Vertical Jump Height (OptoJump) | Vertical jump height was assessed using the OptoJump system during single-leg vertical jump tasks. | At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6) |
| Vertical Jump Power (OptoJump) | Vertical jump power was measured using the OptoJump system to evaluate lower extremity explosive strength. | At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6) |
| Reactive Strength Index (RSI, OptoJump) | RSI was calculated using the OptoJump system to assess neuromuscular efficiency during jump tasks. | At baseline (Day 1) and following completion of 6 weeks of intervention (Week 6) |