Effects of Progressive Neuromuscular Stabilization Exercises Versus Aerobic Exercises on Body Composition and Postural Balance in Children With Obesity
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In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Progressive Neuromuscular Stabilization Exercise, Aerobic Exercise.
- Who it may be relevant to
- Registry conditions: Childhood Obesity, Aerobic Exercise, Exercise. Basic parameters: 12 years — 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effects of Progressive Neuromuscular Stabilization Exercises Versus Aerobic Exercises on Body Composition and Postural Balance in Children With Obesity: A Randomized Controlled Trial
Overview
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.
Detailed description
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.
Interventions
- Other Progressive Neuromuscular Stabilization Exercise
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. - Other Aerobic Exercise
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.
Primary outcome measures
- Change in Overall Stability Index (OSI) [Time frame: Baseline and post-intervention (Week 12)]
- Change in Anterior-Posterior Stability Index (APSI) [Time frame: Baseline and post-intervention (Week 12)]
- Change in Medial-Lateral Stability Index (MLSI) [Time frame: Baseline and post-intervention (Week 12)]
Secondary outcome measures (12)
- Change in Body Mass Index [Time frame: Baseline and post-intervention (Week 12)]
- Change in Waist Circumference [Time frame: Baseline and post-intervention (Week 12)]
- Change in Skinfold Thickness [Time frame: Baseline and post-intervention (Week 12)]
- Change in Body Fat Percentage [Time frame: Baseline and post-intervention (Week 12)]
- Change in Prone Plank Duration [Time frame: Baseline and post-intervention (Week 12)]
- Change in Side Plank Duration [Time frame: Baseline and post-intervention (Week 12)]
- Change in 6-Minute Walk Test Distance [Time frame: Baseline and post-intervention (Week 12)]
- Change in 30-Second Sit-to-Stand Test [Time frame: Baseline and post-intervention (Week 12)]
- Change in 20-Meter Shuttle Run Performance [Time frame: Baseline and post-intervention (Week 12)]
- Change in Physical Activity Level [Time frame: Baseline and post-intervention (Week 12)]
- Change in Self-Perception [Time frame: Baseline and post-intervention (Week 12)]
- Change in Health-Related Quality of Life [Time frame: Baseline and post-intervention (Week 12)]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Turkey (Türkiye) · 1 center
- Istanbul University- Cerrahpasa — Istanbul
Publications
- Men J, Wang P, Gao Q, Li Y, Zhu G, Yu Z, Wu S, Zhang Y, An W, Wang J, Wu Y, Li Z, Zhang J. Impact of exercise on anthropometric outcomes in children and adolescents with overweight or obesity: a systematic review and meta-analysis based on 113 randomized controlled trials worldwide. BMC Public Health. 2025 Jul 7;25(1):2400. doi: 10.1186/s12889-025-23413-9. PMID 40624670
- Bataweel EA, Ibrahim AI. Balance and musculoskeletal flexibility in children with obesity: a cross-sectional study. Ann Saudi Med. 2020 Mar-Apr;40(2):120-125. doi: 10.5144/0256-4947.2020.120. Epub 2020 Apr 2. PMID 32241174
- Kc S, Goyal M, Sharma S, Goyal K. Balance training exercises and postural control in overweight and obese children: A systematic review. J Bodyw Mov Ther. 2025 Jun;42:344-351. doi: 10.1016/j.jbmt.2024.12.036. Epub 2024 Dec 28. PMID 40325690
Identifiers
NCT: NCT07744022 · 25.06.2026-1665933