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临床试验/NCT03172962
NCT03172962已完成不适用

Effect of Strength Training for Chronic Low Back Pain Patients: Randomized Clinical Trial

National Research Centre for the Working Environment, Denmark2 个研究点 分布在 1 个国家目标入组 85 人开始时间: 2017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
状态
已完成
发起方
入组人数
85
试验地点
2
主要终点
Back pain recurrence

研究概览

简要总结

Low back pain (LBP) is common in the population and has great socioeconomic consequences for societies across Europe and the United States. About a third of working-age adults have frequent LBP, and for about 10% the pain becomes chronic with consequences for work and leisure activities. A Cochrane review from April 2017 concluded that physical exercise is an intervention with few adverse events and positive outcomes on pain and function in adults with chronic pain. However, when scrutinizing the specific studies of the review there are large differences in adherence to the exercise interventions and consequently in the results obtained. Thus, there is a need for simple exercises that the patients can easily adhere to.

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
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Non-specific Chronic low back pain patient (more than 3 months) at the hospital Arnau de Vilanova

排除标准

  • Spine surgery
  • neurologic or psyquiatric disorders
  • Low back traumastism
  • Recent participation in a similar training program

研究组 & 干预措施

Strength training

Experimental

Specific strength training exercises for the lumbar and abdominal muscles for 8 weeks

干预措施: Strength training (Behavioral)

Strength training

Experimental

Specific strength training exercises for the lumbar and abdominal muscles for 8 weeks

干预措施: Usual care (control) (Behavioral)

Usual care (control)

Active Comparator

Will receive the usual care at the hospital

干预措施: Usual care (control) (Behavioral)

结局指标

主要结局

Back pain recurrence

时间窗: 1 to 100 days, beginning from the last day of termination of the 8-week intervention

number of episodes with back pain recurrence after termination of the intervention

Low back pain intensity

时间窗: change from baseline to 8-week follow-up

Low back pain intensity (VAS 0-10)

次要结局

  • Pain sites(change from baseline to 8-week follow-up)
  • Use of analgesics(change from baseline to 8-week follow-up)
  • Muscle endurance(change from baseline to 8-week follow-up)
  • Roland-Morris disability(change from baseline to 8-week follow-up)
  • Handgrip strength(change from baseline to 8-week follow-up)

研究者

发起方
National Research Centre for the Working Environment, Denmark
申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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