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临床试验/NCT02276794
NCT02276794终止不适用

The Effects of Thrust Versus Non-thrust Manipulation on Pain, Trunk Proprioception and Postural Stability in Subjects With Chronic Low Back Pain

Federal University of Health Science of Porto Alegre2 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2014年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
23
试验地点
2
主要终点
Pain

研究概览

简要总结

This study aims to verify the effects of Thrust Versus Non-thrust Manipulation on Pain, Trunk Proprioception and Postural Stability in Subjects With Chronic Low Back Pain.

详细描述

Forty individuals with chronic low back pain will be randomly assigned, by a researcher not involved in data collection, to two treatment groups: Thrust manipulation (side-lying rotational manipulation standardized to the L4-L5 level) or non-thrust manipulation (side-lying grade III rotational non-thrust manipulation). A single treatment session will be provided.

Outcome measurement will be conducted immediately after the treatment session. Data will be collected by a blinded assessor. Between-group differences will be calculated by constructing mixed linear models following an intention-to-treat principle.

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

入选标准

  • Age greater than 18 years
  • Chronic Low back pain (pain lasting for at least 12 weeks)

排除标准

  • Previous surgery or fracture at the lumbar spine
  • Pregnancy
  • Inflammatory disorders
  • Symptoms distal to the gluteal line
  • Having received manipulative treatment in the past four weeks

结局指标

主要结局

Pain

时间窗: Up to 10 minutes after intervention

Pain will me measured Up to 10 minutes after intervention by an 11 point (0-11) Numeric Pain Rating Scale (NPRS)

次要结局

  • Global Perceived Effect(Up to 10 minutes after intervention)
  • Lumbar joint position sense(Up to 10 minutes after intervention)
  • Peak plantar pressure(Up to 10 minutes after intervention)
  • Center of Pressure displacement(Up to 10 minutes after intervention)

研究者

发起方
Federal University of Health Science of Porto Alegre
申办方类型
Other
责任方
Principal Investigator
主要研究者

Giovanni Esteves Ferreira

PT

Federal University of Health Science of Porto Alegre

研究点 (2)

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