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临床试验/NCT07103499
NCT07103499已完成不适用

Effects of Abdominal Endurance and Core Stabilization Exercises on Respiratory Functions in Overweight and Obese Women

Ondokuz Mayıs University4 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2025年6月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
54
试验地点
4
主要终点
Forced Vital Capacity (FVC) - Spirometry

研究概览

简要总结

This study aims to examine the effects of an 8-week Pilates-based exercise program on breathing functions in overweight and obese women (BMI ≥ 25). The program includes exercises for abdominal endurance and core stabilization, performed three times a week.

Participants will be divided into two groups: an exercise group and a control group. Before and after the program, measurements will include lung function (spirometry), breathing rate, breath-holding time, abdominal mobility, core endurance (curl-up test), and quality of life (SF-36 questionnaire).

The goal is to find out whether this type of exercise can improve breathing and overall health in women with excess weight.

详细描述

This study aims to investigate the effect of an 8-week Pilates-based abdominal endurance and core stabilization exercise program on respiratory function in obese and overweight women (BMI ≥ 25). The intervention program is planned to last for a total of 24 sessions, 3 days a week. The exercises will be performed using reformer and cadillac devices, under the supervision of a physical therapist, at the Easyfiz Healthy Living Center.

Participants will be randomly assigned to two groups: an experimental group receiving the exercise intervention and a control group not receiving the intervention. Assessments conducted before and after the study for both groups will include the following parameters:

  • Spirometry (FEV₁, FVC, FEV₁/FVC ratio),
  • Respiratory rate,
  • Breath-holding time (in seconds),
  • Thoracoabdominal expansion (measured with a tape measure at the epigastric, subcostal, and lower costal levels),
  • Core muscle endurance (using the ACSM Curl-Up test),
  • Quality of life (using the 36-item Short Form - SF-36).

The exercise program will be planned in three phases:

Weeks 1-2: beginner level, Weeks 3-5: intermediate level, Weeks 6-8: advanced level. Each session will last approximately 45-50 minutes and will consist of a warm-up (diaphragmatic breathing and mobilization), main exercise (core stability and breathing-focused movements), and cool-down (stretching and breathing relaxation exercises).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women aged 18-60
  • Body mass index (BMI) ≥ 25 kg/m² (obese and overweight)
  • Baseline FEV0 value ≥ 80% (measured by spirometry)
  • Individuals without respiratory disease (no diagnosis of asthma, COPD, etc.)
  • Individuals who have not engaged in regular exercise in the past 6 months
  • Individuals without orthopedic or neurological conditions that physically prevent participation in the exercise protocol
  • Non-pregnant individuals
  • Individuals who voluntarily agree to participate in the study and sign the informed consent form

排除标准

  • 1. Individuals with a FEV0 value <80% (due to risk of obstructive lung disease)
  • Individuals who have undergone surgery in the abdomen, waist, or pelvic area within the last 6 months
  • Individuals with orthopedic, neurological, or systemic diseases that would prevent them from exercising
  • Individuals who have been engaging in regular exercise for 3 or more days per week in the past 3 months
  • Individuals with diagnosed respiratory diseases (e.g., asthma, COPD, etc.)
  • Individuals who are unable to comply with the exercise program due to psychiatric diagnosis or communication difficulties

研究组 & 干预措施

Control Group

No Intervention

Participants in this group will not receive any specific exercise or breathing intervention. They will be instructed to maintain their usual daily activities during the study period.

Intervention Group

Experimental

This group will participate in an 8-week supervised Pilates-based exercise program focused on core stabilization and abdominal endurance. Sessions will be held three times a week at Easyfiz Clinic using reformer and cadillac Pilates equipment. Each session will include diaphragmatic breathing-based warm-up and cool-down components.

干预措施: Pilates-Based Core and Breathing Exercise Program (Behavioral)

结局指标

主要结局

Forced Vital Capacity (FVC) - Spirometry

时间窗: Baseline and at 8 weeks after the intervention

Forced Vital Capacity (FVC) - Spirometry

时间窗: Baseline and immediately after the 8-week intervention

Forced vital capacity (FVC) was assessed using spirometry and expressed in liters (L). FVC represents the maximum volume of air that can be forcibly exhaled after a maximal inspiration.

Forced Expiratory Volume in 1 Second (FEV₁) - Spirometry

时间窗: Baseline and immediately after the 8-week intervention

Forced expiratory volume in one second (FEV₁) was assessed using spirometry and expressed in liters (L). FEV₁ represents the volume of air forcibly exhaled during the first second of a forced expiratory maneuver following maximal inspiration.

FEV₁/FVC Ratio - Spirometry

时间窗: Baseline and immediately after the 8-week intervention

The FEV₁/FVC ratio was calculated from spirometric measurements as the ratio of forced expiratory volume in one second (FEV₁) to forced vital capacity (FVC) and expressed as a percentage (%)

Peak Expiratory Flow Rate (PEFR) - Spirometry

时间窗: Baseline and immediately after the 8-week intervention

Peak expiratory flow rate (PEFR) was assessed using spirometry and expressed in liters per second (L/s). PEFR represents the maximum expiratory flow achieved during a forced expiratory maneuver following maximal inspiration.

Upper Thoracic Expansion (Upper Chest Mobility)

时间窗: Baseline and immediately after the 8-week intervention

Upper thoracic expansion (upper chest mobility) was assessed using a tape measure and expressed in centimeters (cm). The difference in chest circumference between maximal inspiration and maximal expiration was recorded to evaluate upper thoracic mobility.

次要结局

未报告次要终点

研究者

发起方
Ondokuz Mayıs University
申办方类型
Other
责任方
Principal Investigator
主要研究者

MİNE PEKESEN KURTÇA

Ass.Prof.

Ondokuz Mayıs University

研究点 (4)

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