跳至主要内容
临床试验/NCT04099654
NCT04099654已完成不适用

The Effect of Structured Core Stabilization Exercise Program on Functional Capacity, Physical Fitness and Quality of Life in Obese Subjects Awaiting Bariatric Surgery: a Randomized Controlled Trial

Istanbul University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2019年9月30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
入组人数
30
试验地点
1
主要终点
Assessment of Core Stabilization

研究概览

简要总结

In this study, our primary aim is to investigate the effects of structured core stabilization exercise program on functional capacity, body composition, muscle strength, endurance, balance, quality of life in adult obese individuals expecting bariatric surgery. Our secondary aim is to provide the individual with exercise habits and increase the level of physical activity in daily life with the exercise program planned according to the needs of the individual.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Individuals aged between 18-65
  • •BMI ≥30 kg/m2, individuals waiting bariatric surgery
  • •No surgical operation in the last 6 months

排除标准

  • •Musculoskeletal disorders or systemic diseases that may prevent exercise
  • •The presence of psychiatric or neurological disease affecting cooperation and cognitive functions
  • •Presence of acute pain
  • •Heart pain
  • •Presence of previous myocardial infarction, subjective heart failure, uncontrolled diabetes and hypertension
  • •Regular exercise for 6 months

研究组 & 干预措施

Counseling of physical activity

Experimental

干预措施: Counseling of physical activity (Other)

Core-Stabilization Exercise

Experimental

干预措施: Core-Stabilization Exercise (Other)

结局指标

主要结局

Assessment of Core Stabilization

时间窗: Change from baseline to 8 weeks, follow up at two months

Core stabilization evaluation will be done with Anterior and Side Abdominal Strength Tests, Trunk Flexor Test and Modified Push Up Test. These tests will be performed using a 2 kilogram medicine ball. Test positions are supine and sitting position.

Six Minute Walk Test

时间窗: Change from baseline to 8 weeks, follow up at two months

The Six Minute Walk Test was conducted according to a standardized protocol, using an internal hallway with the 30-meter distance marked by colored tape on the floor. Participants will be told that "the purpose of this test is to see how far you can walk in six minutes." Then, they will be instructed to "walk from end to end of the hallway at your own pace, in order to cover as much ground as possible." Participants will be allowed to stop and rest during the test, but will be instructed to resume walking as soon as they were able to do so. Before the walk started and at the end of the 6-min walk, participants will be shown a modified Borg dyspnea scale printed on a card and asked to "indicate your current degree of shortness of breath" on a scale of "0 = nothing at all" to "10 = very, very severe." At the end of the walk, they will be asked if they had experienced any of the following specific symptoms: dyspnea, chest pain, light-headedness, or leg pain, or any other symptoms.

次要结局

  • Bioelectrical Impedance Analysis-obesity score(Change from baseline to 8 weeks, follow up at two months)
  • Biodex Balance System-Fall Risk Test(Change from baseline to 8 weeks, follow up at two months)
  • Obesity Specific Quality of Life Scale(Change from baseline to 8 weeks, follow up at two months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Saime Nilay Arman

Assist.Prof.Dr.

Istanbul University

研究点 (1)

Loading locations...

相似试验