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临床试验/NCT02633917
NCT02633917已完成不适用

Motor Control Exercises vs Standard Exercises in Patients With Unspecific Low Back Pain

Universidad Complutense de Madrid0 个研究点目标入组 84 人开始时间: 2011年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
84
主要终点
Change in pain level from baseline at one month and three months after the intervention, measured with a visual analogic scale.

研究概览

简要总结

The purpose of the present study was to evaluate and compare the effects of motor control exercises and standard exercises in the pain, incapacity and medicine intake of subjects with unspecific low-back pain.

详细描述

Eighty-four subjects with unspecific low-back pain were randomly recruited for the present study. The subjects were randomly allocated into control group (who received one hour of standard physiotherapy exercises every days during ten days) or intervention group (who received one hour of control motor exercises every days during ten days). One month after finishing these ten days, patients should perform a home-based exercises program during two months (control group performed home-based standard physiotherapy exercises; intervention group performed home-based motor control exercises). Pain (visual analogic scale), incapacity index (Roland Morris questionnaire) and medicine intake (diary) were evaluated before the intervention, one month and three months after ending the first ten days of intervention.

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
Triple (Participant, Investigator, Outcomes Assessor)

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

入选标准

  • subjects should be independent to walk
  • subjects should have unspecific low back pain during at least the last two months
  • subjects should have had at least two recidives of low back pain within the last year

排除标准

  • subjects with concomitant pathologies that impede the performance of exercises
  • pregnants
  • subjects with oncologic pathologies
  • subjects with cognitive alterations that impede the understanding of the tests

结局指标

主要结局

Change in pain level from baseline at one month and three months after the intervention, measured with a visual analogic scale.

时间窗: The day before beginning the intervention, one month and three months after the first ten days of intervention

Visual analogic scale

次要结局

  • Change in incapacity index from baseline at one month and three months after the intervention, measured with the Roland Morris questionnaire.(The day before beginning the intervention, one month and three months after the first ten days of intervention)
  • Change in medication intake from baseline at one month and three months after the intervention, measured with a diary that subjects should complete.(The day before beginning the intervention, one month and three months after the first ten days of intervention)

研究者

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

Gustavo Plaza Manzano

Director

Universidad Complutense de Madrid

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