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Effects of Progressive Neuromuscular Stabilization Exercises Versus Aerobic Exercises on Body Composition and Postural Balance in Children With Obesity

2 sierpnia 2026 zaktualizowane przez: Emine Dilek Kurbaloğlu, Istanbul University - Cerrahpasa

Effects of Progressive Neuromuscular Stabilization Exercises Versus Aerobic Exercises on Body Composition and Postural Balance in Children With Obesity: A Randomized Controlled Trial

Introduction: Childhood obesity can impair postural control, balance, and motor skills, thereby limiting participation in physical activity. Aerobic exercise is widely used to improve cardiovascular fitness and support weight management in children with obesity. In recent years, however, Progressive Neuromuscular Stabilization (PNS) exercises, which aim to retrain the neuromuscular system, have been suggested to have beneficial effects on core stability, balance, and postural control. Technology-assisted exercise interventions may increase children's participation and enhance motivation throughout the rehabilitation process. This study aims to compare the effectiveness of technology-assisted PNS exercises with conventional aerobic exercise in children with obesity.

Methods: This study will be conducted among children attending the Department of Pediatrics, Istanbul University-Cerrahpaşa who meet the eligibility criteria. Children aged 12-18 years with obesity will be recruited. Participants will be randomly allocated into three groups: the Aerobic Exercise (AE) group, the Progressive Neuromuscular Stabilization (PNS) group, and the Control group.

Participants in the exercise groups will receive supervised exercise sessions twice weekly for 12 weeks in a clinical setting and will be instructed to perform home-based exercises on the remaining days. Home exercise programs will be delivered through the BeCure® mobile application, where exercise videos will be uploaded, and participants will be asked to perform progressively advancing exercises on a weekly basis. The control group will receive a single session of exercise counseling. Outcome assessments will be performed before and after the intervention.

Sample Size: The sample size was calculated using G*Power version 3.1. Based on moderate effect sizes reported in the literature (Lengkana et al., 2019), the effect size was set at f = 0.30, with a significance level of α = 0.05 and statistical power of 1 - β = 0.95. Power analysis for a repeated-measures design with three groups and two measurement time points (baseline and post-intervention) indicated a minimum total sample size of 48 participants. To account for potential dropouts, a total of 54 participants will be recruited. Participants will be assigned to the study groups using block randomization stratified by age and sex.

Primary Outcome Measure:

Balance and postural control will be assessed using the Biodex Balance System.

Secondary Outcome Measures:

Body composition will be evaluated using Body Mass Index (BMI), triceps and subscapular skinfold thickness, waist circumference, and Bioelectrical Impedance Analysis (BIA) to determine body fat percentage. Core muscle endurance will be assessed using the Prone Plank Test and the Side Plank Test. Functional performance will be evaluated using the 6-Minute Walk Test (6MWT), the 30-Second Sit-to-Stand Test (30-s STS), and the 20-Meter Shuttle Run Test.

Physical activity level will be assessed using the Physical Activity Questionnaire for Children (PAQ-C). Self-perception and body image will be evaluated using the Self-Perception Profile for Children (SPPC). Health-related quality of life will be assessed using the Pediatric Quality of Life Inventory (PedsQL), while fatigue will be evaluated using the PedsQL Multidimensional Fatigue Scale. Posture will be assessed using the New York Posture Rating Scale.

Study Plan:

Each exercise session will last approximately 40 minutes, consisting of a 5-minute warm-up, 30 minutes of the main exercise program, and a 5-minute cool-down.

Przegląd badań

Szczegółowy opis

Detailed Study Description Background

Childhood obesity is a major global public health concern associated with numerous adverse health outcomes, including metabolic, cardiovascular, and musculoskeletal disorders. Beyond these well-recognized complications, obesity negatively affects postural control, balance, motor performance, and functional movement capacity. Excess body weight alters biomechanical alignment, shifts the center of gravity, and impairs neuromuscular coordination, thereby increasing postural instability and reducing participation in physical activity. Consequently, children with obesity often develop a sedentary lifestyle, which further exacerbates obesity and its associated health risks.

Aerobic exercise is widely recommended as a first-line intervention for childhood obesity because of its well-established benefits in improving cardiovascular fitness, energy expenditure, body composition, and overall physical health. However, aerobic exercise alone may not sufficiently address deficits in neuromuscular control, postural stability, and core muscle function, which are common in children with obesity.

Progressive Neuromuscular Stabilization (PNS) exercises are based on the principles of developmental kinesiology and progressive motor control training. These exercises aim to improve postural alignment, enhance core stability, optimize neuromuscular coordination, and restore efficient movement patterns through progressively challenging stabilization tasks. Recent evidence suggests that neuromuscular stabilization exercises may improve balance, postural control, movement quality, and functional performance in pediatric populations. Nevertheless, evidence regarding their effectiveness in children with obesity remains limited.

In addition, adherence to long-term exercise programs represents one of the greatest challenges in pediatric obesity management. Technology-assisted exercise interventions delivered through mobile applications may increase exercise adherence by providing structured guidance, visual demonstrations, progressive exercise progression, and continuous motivation. Therefore, integrating technology-supported home exercise programs with supervised clinical sessions may improve treatment compliance and maximize intervention effectiveness.

This randomized controlled trial aims to compare the effects of technology-assisted Progressive Neuromuscular Stabilization exercises and conventional aerobic exercise on balance, postural control, body composition, functional performance, and quality of life in children with obesity.

Methods

This study will be conducted at the Department of Pediatrics, Istanbul University-Cerrahpaşa, among children referred to the pediatric obesity outpatient clinic. Participants meeting the eligibility criteria will be invited to participate after obtaining written informed consent from their parents or legal guardians and assent from the children.

Children aged 12 to 18 years who are classified as obese according to age- and sex-specific criteria will be enrolled. Eligible participants will be randomly assigned using age- and sex-stratified block randomization into one of three study groups:

Progressive Neuromuscular Stabilization (PNS) Exercise Group Aerobic Exercise (AE) Group Control Group

Both intervention groups will participate in a 12-week exercise program, attending supervised clinical exercise sessions twice weekly. Each session will last approximately 40 minutes, including:

5 minutes of warm-up, 30 minutes of the main exercise program, 5 minutes of cool-down exercises.

In addition to supervised sessions, participants in both intervention groups will perform home-based exercises on the remaining weekdays. Home exercise programs will be delivered through the BeCure® mobile application, where exercise videos prepared specifically for each intervention will be uploaded. Participants will be instructed to complete progressively advancing exercise programs each week. Exercise adherence will be monitored through the mobile application, and participants will receive regular follow-up to encourage compliance.

The PNS intervention will consist of progressively challenging exercises targeting diaphragmatic breathing, trunk stabilization, neuromuscular coordination, developmental movement patterns, proprioception, balance, and postural control. Exercise difficulty will increase throughout the intervention by incorporating unstable surfaces, resistance, dual-task activities, and functional movement progression.

The aerobic exercise program will include age-appropriate rhythmic and functional aerobic activities such as walking, stepping, dynamic movement games, and interval-based exercises. Exercise intensity will be progressively increased according to participants' functional capacity throughout the intervention.

Participants allocated to the control group will receive a single standardized exercise counseling session that includes recommendations regarding healthy lifestyle habits and physical activity but will not participate in the supervised exercise intervention.

Outcome assessments will be performed at baseline and immediately after completion of the 12-week intervention period by assessors blinded to group allocation whenever possible.

Sample Size

Sample size was calculated using G*Power version 3.1 based on previously published findings (Lengkana et al., 2019). Assuming a medium effect size (f = 0.30), a significance level of α = 0.05, and a statistical power of 95% (1-β = 0.95), repeated-measures ANOVA with three groups and two assessment time points required a minimum total sample size of 48 participants. Considering potential dropouts during the intervention, the final planned sample size is 54 participants.

Primary Outcome

The primary outcome of the study is balance and postural control, which will be assessed using the Biodex Balance System. Static and dynamic postural stability indices, including the Overall Stability Index (OSI), Anterior-Posterior Stability Index (APSI), and Medial-Lateral Stability Index (MLSI), will be recorded.

Secondary Outcomes

Secondary outcome measures include:

Body composition Body Mass Index (BMI) Waist circumference Triceps skinfold thickness Subscapular skinfold thickness Body fat percentage measured by Bioelectrical Impedance Analysis (BIA) Core muscle endurance Prone Plank Test Side Plank Test Functional performance 6-Minute Walk Test (6MWT) 30-Second Sit-to-Stand Test 20-Meter Shuttle Run Test Physical activity level Physical Activity Questionnaire for Children (PAQ-C) Self-perception and body image Self-Perception Profile for Children (SPPC) Health-related quality of life Pediatric Quality of Life Inventory (PedsQL) Fatigue Pediatric Quality of Life Inventory Multidimensional Fatigue Scale Postural assessment New York Posture Rating Scale Expected Significance

This study will provide evidence regarding the comparative effectiveness of technology-assisted Progressive Neuromuscular Stabilization exercises and conventional aerobic exercise in children with obesity. The findings may contribute to the development of more comprehensive rehabilitation strategies that not only improve body composition but also enhance balance, postural control, neuromuscular function, functional capacity, and exercise adherence. Furthermore, integrating mobile application-based home exercise programs into pediatric obesity rehabilitation may offer a practical and sustainable approach for increasing long-term participation in physical activity and improving treatment outcomes.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

54

Faza

  • Nie dotyczy

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

  • Nazwa: Emine Dilek Kurbaloğlu, PhD Student
  • Numer telefonu: +905416258918
  • E-mail: fzt.edilek@gmail.com

Kopia zapasowa kontaktu do badania

Lokalizacje studiów

      • Istanbul, Turcja (Türkiye)
        • Rekrutacyjny
        • Istanbul University- Cerrahpasa
        • Kontakt:

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dziecko
  • Dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  • Aged 12 to 18 years
  • Classified as having Class I obesity (Body Mass Index [BMI] ≥95th percentile and <120% of the 95th percentile for age and sex) or Class II obesity (BMI ≥120% and <140% of the 95th percentile for age and sex), according to the Centers for Disease Control and Prevention (CDC) age- and sex-specific growth charts.
  • Able to maintain a single-leg stance on the non-dominant leg with eyes closed for less than 30 seconds.
  • Written informed consent provided by a parent or legal guardian, and assent obtained from the participant.
  • Willing and able to participate in the study.

Exclusion Criteria:

  • Classified as having Class III obesity (Body Mass Index [BMI] ≥140% of the 95th percentile for age and sex).
  • Presence of an orthopedic condition that would prevent participation in the exercise program.
  • History of any injury or surgery within the previous 6 months.
  • Presence of a chronic neurological disorder.
  • Presence of a psychiatric disorder.
  • Presence of a severe cognitive impairment.
  • Presence of cardiovascular disease.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Randomizowane
  • Model interwencyjny: Przydział równoległy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Progressive Neuromuscular Stabilization (PNS) Exercise Group

Participants assigned to the Progressive Neuromuscular Stabilization (PNS) group will participate in a 12-week exercise program consisting of supervised clinical sessions twice weekly and technology-assisted home-based exercises on the remaining weekdays. The exercise program will progressively target diaphragmatic breathing, core stabilization, neuromuscular coordination, balance, postural control, proprioception, and functional movement patterns. Exercise difficulty will gradually increase by incorporating unstable surfaces, resistance exercises, dual-task activities, and dynamic functional tasks. Home exercises will be delivered through the BeCure® mobile application using progressively updated instructional videos.

Intervention Behavioral: Progressive Neuromuscular Stabilization Exercise A progressive neuromuscular exercise program designed to improve core stability, postural control, balance, proprioception, and neuromuscular coordination through supervised and home-based exerc

Progressive Neuromuscular Stabilization Exercise

Participants will complete a 12-week Progressive Neuromuscular Stabilization (PNS) exercise program consisting of supervised clinical sessions twice weekly and home-based exercises delivered through the BeCure® mobile application. The program is designed to improve core stability, balance, postural control, and neuromuscular coordination through progressively challenging exercises.

Eksperymentalny: Aerobic Exercise Group

Participants assigned to the aerobic exercise group will complete a 12-week exercise program consisting of supervised clinical sessions twice weekly and home-based aerobic exercise on the remaining weekdays. The intervention will include age-appropriate aerobic activities such as walking, stepping exercises, dynamic movement games, rhythmic exercises, and interval training. Exercise intensity will be progressively increased according to participants' functional capacity. Home exercise sessions will be delivered through the BeCure® mobile application using weekly exercise videos.

Intervention

Aerobic Exercise

A progressive aerobic exercise program designed to improve cardiovascular fitness, physical activity level, functional capacity, and body composition through supervised and home-based exercise over a 12-week period.

Aerobic Exercise

Participants will complete a 12-week aerobic exercise program consisting of supervised clinical sessions twice weekly and home-based exercises delivered through the BeCure® mobile application. The program includes progressive aerobic activities aimed at improving cardiovascular fitness, physical activity level, and body composition.

Brak interwencji: Control Group

Participants assigned to the control group will receive a single standardized exercise counseling session at baseline regarding healthy lifestyle behaviors and physical activity recommendations. No supervised exercise intervention or structured home exercise program will be provided during the 12-week study period. Participants will continue their usual daily activities.

Intervention

Control Group

Participants will receive a one-time standardized counseling session including education on healthy lifestyle behaviors, physical activity recommendations, and obesity management.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Change in Overall Stability Index (OSI)
Ramy czasowe: Baseline and post-intervention (Week 12)
Overall postural stability will be assessed using the Biodex Balance System. Lower scores indicate better postural stability.
Baseline and post-intervention (Week 12)
Change in Anterior-Posterior Stability Index (APSI)
Ramy czasowe: Baseline and post-intervention (Week 12)
Anterior-posterior postural stability will be assessed using the Biodex Balance System. Lower scores indicate better stability.
Baseline and post-intervention (Week 12)
Change in Medial-Lateral Stability Index (MLSI)
Ramy czasowe: Baseline and post-intervention (Week 12)
Medial-lateral postural stability will be assessed using the Biodex Balance System. Lower scores indicate better stability.
Baseline and post-intervention (Week 12)

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Change in Body Mass Index
Ramy czasowe: Baseline and post-intervention (Week 12)
Body mass index will be calculated by dividing body weight in kilograms by height in meters squared.
Baseline and post-intervention (Week 12)
Change in Waist Circumference
Ramy czasowe: Baseline and post-intervention (Week 12)
Waist circumference will be measured in centimeters using a non-elastic measuring tape.
Baseline and post-intervention (Week 12)
Change in Skinfold Thickness
Ramy czasowe: Baseline and post-intervention (Week 12)
Triceps and subscapular skinfold thickness will be measured in millimeters using a skinfold caliper.
Baseline and post-intervention (Week 12)
Change in Body Fat Percentage
Ramy czasowe: Baseline and post-intervention (Week 12)
Body fat percentage will be assessed using bioelectrical impedance analysis.
Baseline and post-intervention (Week 12)
Change in Prone Plank Duration
Ramy czasowe: Baseline and post-intervention (Week 12)
Core muscle endurance will be assessed by recording the maximum time, in seconds, that the participant can maintain the prone plank position with correct alignment.
Baseline and post-intervention (Week 12)
Change in Side Plank Duration
Ramy czasowe: Baseline and post-intervention (Week 12)
Lateral core muscle endurance will be assessed by recording the maximum time, in seconds, that the participant can maintain the side plank position.
Baseline and post-intervention (Week 12)
Change in 6-Minute Walk Test Distance
Ramy czasowe: Baseline and post-intervention (Week 12)
Functional exercise capacity will be assessed by measuring the total distance, in meters, walked during the 6-Minute Walk Test.
Baseline and post-intervention (Week 12)
Change in 30-Second Sit-to-Stand Test
Ramy czasowe: Baseline and post-intervention (Week 12)
Lower-extremity functional performance will be assessed by recording the number of correctly completed sit-to-stand repetitions within 30 seconds.
Baseline and post-intervention (Week 12)
Change in 20-Meter Shuttle Run Performance
Ramy czasowe: Baseline and post-intervention (Week 12)
Cardiorespiratory fitness will be assessed using the 20-Meter Shuttle Run Test. Performance will be recorded according to the number of completed stages, laps, or total distance.
Baseline and post-intervention (Week 12)
Change in Physical Activity Level
Ramy czasowe: Baseline and post-intervention (Week 12)
Physical activity level will be assessed using the Physical Activity Questionnaire for Children. Higher scores indicate a higher level of physical activity.
Baseline and post-intervention (Week 12)
Change in Self-Perception
Ramy czasowe: Baseline and post-intervention (Week 12)
Self-perception will be assessed using the Self-Perception Profile for Children. Higher scores indicate more positive self-perception.
Baseline and post-intervention (Week 12)
Change in Health-Related Quality of Life
Ramy czasowe: Baseline and post-intervention (Week 12)
Health-related quality of life will be assessed using the Pediatric Quality of Life Inventory. Higher scores indicate better health-related quality of life.
Baseline and post-intervention (Week 12)
Change in Fatigue
Ramy czasowe: Baseline and post-intervention (Week 12)
Fatigue will be assessed using the Pediatric Quality of Life Inventory Multidimensional Fatigue Scale. Higher scores indicate fewer fatigue-related problems.
Baseline and post-intervention (Week 12)
Change in Posture
Ramy czasowe: Baseline and post-intervention (Week 12)
Posture will be assessed using the New York Posture Rating Scale. Higher scores indicate better postural alignment.
Baseline and post-intervention (Week 12)

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Krzesło do nauki: Emine Dilek Kurbaloğlu, PhD Student, Istanbul University - Cerrahpasa

Publikacje i pomocne linki

Osoba odpowiedzialna za wprowadzenie informacji o badaniu dobrowolnie udostępnia te publikacje. Mogą one dotyczyć wszystkiego, co jest związane z badaniem.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Rzeczywisty)

3 lipca 2026

Zakończenie podstawowe (Szacowany)

15 stycznia 2027

Ukończenie studiów (Szacowany)

15 sierpnia 2027

Daty rejestracji na studia

Pierwszy przesłany

26 lipca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

2 sierpnia 2026

Pierwszy wysłany (Rzeczywisty)

4 sierpnia 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

4 sierpnia 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

2 sierpnia 2026

Ostatnia weryfikacja

1 sierpnia 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Opis planu IPD

Individual participant data collected during this study will not be made publicly available because the study involves minors and contains sensitive personal and health information.

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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