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临床试验/NCT01362049
NCT01362049已完成不适用

Mechanisms of Specific Trunk Exercises in Low Back Pain

University of Vermont2 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2010年3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
102
试验地点
2
主要终点
Change From Baseline in Oswestry Disability Scale (0-100%)

研究概览

简要总结

The research objective is to determine which physical therapy (PT) treatment is the most efficacious for patients with lower back pain (LBP), who have been subgrouped based on certain clinical features. There is only limited evidence that supports any one PT treatment for patients with LBP since PT treatment outcomes for exercise protocols are equivocal, given the heterogeneous clinical features of patients with LBP. Thus, classification of patients with LBP into subgroups with shared clinical features has been identified as a research priority by several groups in order to prescribe the most efficacious PT treatment for each homogeneous subgroup. The investigators hypothesize that particular PT treatments are most efficacious when applied to patients with LBP, who present with particular clinical and neuromuscular features.

详细描述

The proposed studies focus on 2 schemas to classify LBP: 1) the Treatment-Based Classification (TBC) system, from which clinical prediction rules about who is most likely to benefit from spinal stabilization exercises (among others) have been developed, and 2) the Movement System Impairment-Based Classification (MSI) system, which includes 5 classifications of LBP named for the specific direction(s) of movements and alignments associated with the person's LBP.

The primary purpose of this proposal is to conduct a prospective, randomized, controlled Phase II clinical trial in order to examine whether or not treatment matched to a patient's specific signs and symptoms (patient-matched) per the TBC is more effective than the MSI system for improving short- (6 weeks) and long-term (12 and 24 months) outcomes in people with chronic LBP. A secondary purpose is to identify prognostic factors that predict clinical outcomes in the 2 treatment groups being compared.

Subjects will be assigned to one of two study arms:

  1. eligible for Treatment-Based Classification (TBC) stabilization exercises based on current criteria ('Eligible' Subject Group); and
  2. subjects who are not eligible for the TBC-based stabilization exercises ('Ineligible' Subject Group).

Within in each study arm, subjects will be randomly assigned to 1 of 2 exercise protocols for a 6-week period:

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
21 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • a history of chronic LBP with or without recurrences for a minimum of 12 months;
  • between 21 - 55 years of age;
  • able to stand and walk without assistance;
  • have an Oswestry Disability Score of 19% or higher AND/OR less than an 8 on one activity reported on the Patient Specific Functional Scale,

排除标准

  • any major structural spinal deformity including scoliosis, kyphosis, or stenosis;
  • spinal fracture or dislocation;
  • osteoporosis;
  • ankylosing spondylitis;
  • rheumatoid arthritis;
  • disc herniation with corroborating clinical signs and symptoms;
  • serious spinal complications such as tumor or infection;
  • previous spinal surgery;
  • frank neurological loss, i.e., weakness and sensory loss;
  • pain or paresthesia below the knee;
  • etiology of LBP other than the lumbar spine, e.g., hip joint;
  • history of neurological disease which required hospitalization;
  • active treatment for cancer;
  • history of unresolved cancer;
  • pregnancy or less than 6 months post-partum or less than 6 months post weaning;
  • magnified symptom-behavior;
  • worker's compensation or disability case;
  • in litigation for the LBP problem;
  • have a BMI ≥ 30.

结局指标

主要结局

Change From Baseline in Oswestry Disability Scale (0-100%)

时间窗: Baseline and 12 Months

Disability; Sacle 0-100% Lower score is considered better/improved

Change From Baseline in Numeric Pain Rating Scale (0-10 Points)

时间窗: Baseline and 12 months

Current Pain Scale 0-10 Lower score is better/improved

次要结局

  • Change From Baseline in SF-36 Health Survey (0-100 Points)(Baseline and 12 months)
  • Change From Baseline in Fear Avoidance Belief Questionnaire (Physical Activity Subscale 0-24 Points)(Baseline and 12 months)
  • Change From Baseline in SF-36 Health Survey (0 - 100 Points)(Baseline and 7 weeks)

研究者

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

Sharon M. Henry

Professor

University of Vermont

研究点 (2)

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