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临床试验/NCT02982382
NCT02982382已完成不适用

Neurophysiological and Functional Effects of Manipulative Therapy and Pain Education in Individuals With Chronic Nonspecific Low Back Pain

Santa Catarina Federal University2 个研究点 分布在 1 个国家目标入组 128 人开始时间: 2016年12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
128
试验地点
2
主要终点
Pain Intensity

研究概览

简要总结

The burden of low back pain more than doubled in the last 20 years, probably caused by biopsychosocial factors. Some noninvasive treatments have been applied in individuals with chronic nonspecific low back pain as spinal manipulation and pain education. However, it is not already clear the neurophysiological effects of these treatments.The purpose of this research is to verify the effects of the technique of spinal manipulation and pain education in individuals with chronic low back pain

详细描述

The outcomes will be subjective pain (measured by Numeric Pain Rating Scale), pressure pain threshold (measured by Algometer), disability (measured by Roland-Morris Disability Questionnaire), fear and avoidance beliefs (measured by Fear Avoidance Beliefs Questionnaire), risk of poor prognosis (measured by STarT Back Screening Tool), quality of life (measured by Short Form-12v2) and blood biomarkers (measured by ELISA). The data will be collected by a blinded assessor.

Individuals eligibility is going to be assessed by blinded assessor to determine if they are or not eligible for this research. Then, they will be informed about the objectives of this study and asked to sign the consent form. Afterward, the sociodemographic data will be recorded. The data related to the research outcomes will be collected by the blinded assessor at baseline assessment, after six weeks and three months.

Random Allocation Before the treatment begins, one of the researchers not involved in the recruiting and assessment will allocate the individuals in one of the groups. Block randomization will be used; it is going to generate by randomization.com, this site will create a list with the randomization sequence, which will be only seen by the physical therapists that will treat the individuals.

Statistical Methods

Sample size calculation The sample size calculation was calculated with the A-priori test with the following specifications: Statistical test ANCOVA, the effect size of 0.25, the statistical power of 80%, and an alpha level of 5%. As a result, the study requires a sample size of 64 per group or 128 individuals in total.

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 (Participant, 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

  • Chronic episodes of nonspecific LBP for at least six months
  • Pain on movement for at least one direction (flexion, extension, side bending or rotation of the trunk)
  • At least score 3 in NPRS.

排除标准

  • Previous history of lumbar myelopathy, rheumatic disease, tumors, peripheral or central neurological disorders
  • Historical of trauma, fracture or surgery in lumbar region;
  • Nerve root compression signs: important muscle weakness affecting lower limb, decrease or abolish of patellar and calcaneus reflex and decrease of dermatomes sensibility of lower limbs.

研究组 & 干预措施

Manipulative Treatment

Experimental

Subjects will receive Manipulative Therapy

干预措施: Manipulative Therapy (Other)

Manipulative Treatment

Experimental

Subjects will receive Manipulative Therapy

干预措施: Pain Education (Other)

Pain Education

Sham Comparator

Subjects will receive Pain Education and manual contact over lumbar region

干预措施: Pain Education (Other)

Pain Education

Sham Comparator

Subjects will receive Pain Education and manual contact over lumbar region

干预措施: Sham (Other)

结局指标

主要结局

Pain Intensity

时间窗: 6 weeks after randomization

Numeric Pain Rating Scale (NPRS)

次要结局

  • Pain Intensity(Baseline, 6 weeks and 3 months)
  • Disabilty(baseline, 6 weeks and 3 months)
  • Pressure Pain Threshold(Baseline, 6 weeks and 3 months)
  • Fear and Beliefs about pain(Baseline, 6 weeks and 3 months)
  • Risk of poor prognosis(Baseline, 6 weeks and 3 months)
  • Quality of Life(Baseline, 6 weeks and 3 months)
  • Serum Level of Cytokines(Baseline, 6 weeks)

研究者

发起方
Santa Catarina Federal University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Clecio Vier

Principal Investigator

Santa Catarina Federal University

研究点 (2)

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