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临床试验/NCT00600197
NCT00600197Unknown不适用

The Effectiveness of Biopsychosocial Education on Quality of Life and Disability of Individuals Suffering From Chronic Low Back Pain

Tehran University of Medical Sciences1 个研究点 分布在 1 个国家目标入组 170 人开始时间: 2008年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
170
试验地点
1
主要终点
SF-36, Roland Morris Disability Questionnaire, Quebec back pain disability

研究概览

简要总结

The purpose of this study is to examine whether the biopsychosocial educational program could improve patients' health-related quality of life at 3-6-12-18-24-30 and 36 - month follow up.

详细描述

Little information exists on biopsychosocial educational program as a multidimensional and interdisciplinary program in which Quality Of Life is as an outcome measure. Thus this educational Program designed in this study is a an outpatient program that used a health education approach to empower participants through a process of assessment, education and skill building in three dimensions of physical,mental and social that leading to improved quality of life. The purpose of this study was to examine to what extent this educational Program could improve low back pain patients' HRQOL.

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Low Back Pain lasting more than 12 weeks with or without pain radiating to the legs.
  • •age 18-70 years.

排除标准

  • •Osteoporosis
  • •Newly operation on the back up to 2 years before the beginning of the study
  • •Fresh vertebral fracture
  • •Malignancy
  • •Infection in the back
  • •spondylolisthesis
  • •Problem in understanding Farsi Language

研究组 & 干预措施

back school

Experimental

干预措施: back school (Behavioral)

Back school

Experimental

a kind of educational program for low back pain

干预措施: back school (Behavioral)

结局指标

主要结局

SF-36, Roland Morris Disability Questionnaire, Quebec back pain disability

时间窗: before intervention

次要结局

  • SF-36,Roland Morris Disability Questionnaire, Quebec back pain disability(3-6-12-18-24-30-36 month after intervention)

研究者

申办方类型
Other

研究点 (1)

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