跳至主要内容
临床试验/NCT01557049
NCT01557049已完成不适用

Global Postural Reeducation in Chronic Low Back Pain: an Randomized Controlled Trial

Federal University of São Paulo2 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2008年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
61
试验地点
2
主要终点
Change from baseline in pain

研究概览

简要总结

The purpose of this study is to evaluate the effectiveness of a Global Postural Reeducation (GPR) program in subjects with chronic low back pain.

详细描述

Approximately 80-85% of individuals will experience low back pain during their lifetime. It is one of the major concerns of current health care. There is evidence for the effectiveness of exercise therapy in patients with chronic low back pain. GPR is a physical therapy method developed in France by Philippe Emmanuel Souchard. Although this method is largely used as form of treatment in most countries, few studies showed its clinical effectiveness in chronic low back pain. This is the first randomized controlled trial, with assessor blind that evaluate the GPR effects in chronic low back pain. All outcome measurements are reliability, validated and sensitivity for statistical changes using the Visual Analogic Scale- VAS (0-10cm), Roland Morris Questionary, SF36 (Quality Life Questionary) and Beck Scale (Depression Symptoms).

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)

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

入选标准

  • between 18-65 years age,
  • low back pain (more than 12 weeks) without legs irradiation,
  • pain between 3-8 cm on a visual Analogue scale (0-10cm).

排除标准

  • fibromyalgia,
  • pregnancy,
  • osteoporosis severe,
  • disc herniation,
  • patients who had undergone spinal surgical or physiotherapeutic interventions within 3 months prior to baseline assessment.

结局指标

主要结局

Change from baseline in pain

时间窗: baseline and two follow-up examinations - after 3 and 6 months from baseline

The primary outcome of this study was the measurement of pain assessed with 0-10cm Visual Analogue Scale (VAS). They were collected at baseline and two follow-up examinations after 3 and 6 months from baseline.

次要结局

  • Change from baseline in function(It was collected at baseline and two follow-up examinations after 3 and 6 months from baseline.)

研究者

发起方
Federal University of São Paulo
申办方类型
Other
责任方
Principal Investigator
主要研究者

Priscila Maria Mendonca de Almeida Lawand

physical therapeutic

Federal University of São Paulo

研究点 (2)

Loading locations...

相似试验