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临床试验/NCT07047287
NCT07047287尚未招募不适用

Global Postural Reeducation Versus Pilates in Patients With Non-specific Low Back Pain

Cairo University0 个研究点目标入组 60 人开始时间: 2025年6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
尚未招募
入组人数
60
主要终点
pain intensity

研究概览

简要总结

to compare between Global Postural Reeducation and Pilates mat on pelvic angles, pain intensity, hip flexibility and Functional disability in patients with chronic non-specific low back pain

详细描述

Chronic low back pain is a common health problem in many developed and developing countries. Individuals suffering from chronic low back pain experience major physical, social, mental, and occupational disruptions. It is not only one of the leading causes of pain but also of a costly burden on the health care budget as chronic low back pain leads to a frequent demand for medical services. The majority of patients (up to 90%) are categorized as having nonspecific low back pain.Global postural reeducation (GPR) is a conservative treatment that we can consider as a global postural exercise method, and widely used in physical therapy clinical practice in many countries. Pilates is a concept of body and mind exercise and a system of repetitive exercises including whole-body movements, breathing, centering, rhythm, and concentration. Pilates is a mindful approach exercise that promote strength, stability and is used for health enhancement and in several diseases.

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 (Outcomes Assessor)

盲法说明

opaque sealed envelope

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •18-50 years old, Low back pain for more than 3 months (pain felt between T12 and the gluteal fold).
  • •Patients willing and able to participate in an exercise program safely and without cognitive impairments that would limit their participation.
  • •BMI index smaller than 30 kg/m2
  • •Both male and female gender were included in the study.
  • •Nonspecific, non-radicular (axial) chronic LBP diagnosis (LBP for at least three months).
  • •Visual Analog Scale (VAS) score of 3 or higher

排除标准

  • •History of back surgery
  • •Rheumatologic disorders,
  • •Spine infections
  • •Spine exercise training in the 3 months before the onset of the study.
  • •Under psychiatric care.
  • •Neurological conditions that would interfere with the assessments, such as major sensory changes, and level of consciousness/ understanding
  • •Advanced joint disease.
  • •History of severe physical and nervous system diseases
  • •Unable to cooperate with the study protocols.

研究组 & 干预措施

global postural reeducation exercise

Experimental

Twenty patients suffer from nonspecific low back pain and will be received Global postural reeducation exercise and conventional physiotherapy treatment two times a week for six weeks

干预措施: global postural reeducation exercise (Other)

global postural reeducation exercise

Experimental

Twenty patients suffer from nonspecific low back pain and will be received Global postural reeducation exercise and conventional physiotherapy treatment two times a week for six weeks

干预措施: conventional therapy (Other)

pilates exercises

Experimental

Twenty patients suffer from nonspecific low back pain and will receive Pilates exercise and conventional physiotherapy treatment two times a week for six weeks

干预措施: pilates exercises (Other)

pilates exercises

Experimental

Twenty patients suffer from nonspecific low back pain and will receive Pilates exercise and conventional physiotherapy treatment two times a week for six weeks

干预措施: conventional therapy (Other)

conventional therapy

Active Comparator

Twenty patients suffer from nonspecific low back pain and will receive conventional physiotherapy treatment two times a week for six weeks.

干预措施: conventional therapy (Other)

结局指标

主要结局

pain intensity

时间窗: up to six weeks

VAS is employed as a quantitative tool to assess the subjective intensity of pain experienced by an individual. The VAS is a reliable and valid method for assessing low back pain clinically. It consists of a single handwritten mark down the length of a 10-cm line, with "no pain" at one end of the scale (0 cm) and "worst pain" at the other (10 cm)

次要结局

  • disability(up to six weeks)
  • anterior pelvic tilt(up to six weeks)
  • lumbar lordosis(up to six weeks)
  • hip flexor flexibility(up to six weeks)

研究者

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

ibrahim mostafa mohamed

principle investigator : ibrahim mostafa mohamed

Cairo University

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