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Neuromuscular Balance Exercise Effects in Overweight and Obese Individuals

Investigation of the Effectiveness of Neuromuscular Control-Based Exercises Combined With Aerobic and Strength Training Exercises on Balance in Overweight and Obese Individuals

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07372157
Enrollment
40
Registered
2026-01-28
Start date
2025-06-15
Completion date
2026-06-01
Last updated
2026-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight and Obesity

Keywords

Obesity, Exercise, Neuromuscular control, Quality of life, Postural stability

Brief summary

This randomized controlled study aims to evaluate the effects of adding neuromuscular balance exercises to exercise programs on functional capacity, balance, and physical fitness in individuals with obesity. Forty participants will be randomly assigned to either a control group receiving aerobic and strength training exercises or an intervention group receiving aerobic and strength training combined with neuromuscular balance exercises. Both exercise programs will be conducted three times per week for eight weeks. Functional capacity, balance, and physical fitness outcomes will be assessed at baseline and after the intervention period. The findings are expected to contribute to the integration of balance-focused exercises into rehabilitation programs for individuals with obesity.

Detailed description

This project will begin with initial assessments of volunteers to examine the effects of balance exercises on postural control and neuromuscular connections in obesity treatment. A multimodal exercise program (neuromuscular balance exercises, aerobic training, and resistance training) will be designed for individuals with obesity, and its effects on physical function, balance impairment, and weight management will be evaluated. In the first phase, participants' static and dynamic balance will be analyzed using clinical scales. In the second phase, an 8-week multimodal exercise program will be implemented, and the outcomes will be comparatively examined in relation to the weight loss process. The study aims to provide scientific data to support the individualization of exercise programs by examining postural balance adaptations in response to changes in body composition during weight loss. The findings are expected to contribute to more comprehensive physical activity approaches in obesity management and to guide clinical applications. This study adds a different perspective by evaluating the functional benefits of neuromuscular-based balance exercises in addition to traditional aerobic and strength training exercises. The assessment, conducted in individuals with obesity who have experienced weight loss, is expected to provide important findings for the interpretation and discussion of outcomes.

Interventions

The aerobic and strength training program consists of supervised exercise sessions performed three days per week for eight weeks. Aerobic exercises are conducted at a moderate intensity, and strength training targets major muscle groups using body weight and resistance-based exercises. Each session is structured to include warm-up, main exercise components, and cool-down phases.

BEHAVIORALNeuromuscular balance exercises

Neuromuscular balance exercises are added to the standard exercise program and are designed to improve postural control and balance. The exercises include progressive static and dynamic balance tasks and are performed three times per week for eight weeks under supervision.

Sponsors

Marmara University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

This is an open-label study with no blinding of participants or investigators.

Intervention model description

Participants are randomly assigned to either a control group or an intervention group, and both groups are followed in parallel throughout the study period.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Volunteering to participate in the study * Having a BMI of 25-35 kg/m2 * Not having undergone any surgical operation in the last 6 months

Exclusion criteria

* Any musculoskeletal disorder or systemic disease that would prevent exercise * Balance problems due to any disease that could prevent exercise * Psychiatric or neurological disease affecting cooperation and cognitive functions * Acute pain for any reason * Chest pain * History of myocardial infarction within the last year * Congestive heart failure * Patient's inability to adhere to treatment

Design outcomes

Primary

MeasureTime frameDescription
Dynamic Balance Performance (Four Step Square Test)Baseline, at the 4th weeks and at the end of 8 weeksDynamic balance will be assessed using the Four Step Square Test, which measures the time (in seconds) required to complete a multidirectional stepping sequence.
Postural Control (Functional Reach Test)Baseline, Week 4, and Week 8Postural control will be evaluated using the Functional Reach Test, which measures the maximal forward reach distance (in centimeters) while maintaining a fixed base of support.
Walking Endurance (2-Minute Walk Test)Baseline, at the 4th weeks and at the end of 8 weeksWalking endurance will be assessed using the 2-Minute Walk Test, which measures the total distance walked in meters over a two-minute period.
Lower Extremity Functional Strength (30-Second Chair Stand Test)Baseline, Week 4, and Week 8Lower extremity functional strength will be evaluated using the 30-Second Chair Stand Test, which measures the number of full stands completed within 30 seconds.

Secondary

MeasureTime frameDescription
Health-Related Quality of Life Assessed by the Short Form-12 (SF-12)Baseline, at the 4th weeks and at the end of 8 weeksHealth-related quality of life will be evaluated using the Short Form-12 (SF-12) Health Survey, which assesses physical and mental health components.

Countries

Turkey (Türkiye)

Contacts

CONTACTEkin UĞUR CANÖZ, MSc
ekinugur@marun.edu.tr+905374525191
CONTACTMine Gülden G Polat, PhD
gpolat@marmara.edu.tr+90216 777 57 00
PRINCIPAL_INVESTIGATORMine Gülden G Polat, PhD

Marmara University Faculty of Health Sciences

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026