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临床试验/NCT00916734
NCT00916734已完成3 期

Assessing Patient Response to Therapeutic Exercise Based on the Clinical Prediction Rule for Spinal Manipulation

Daemen College2 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2007年11月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
31
试验地点
2
主要终点
Pain level as measured on numerical pain rating scale

研究概览

简要总结

The purpose of this study is to determine whether patients who meet the criteria of the clinical prediction rule for spinal manipulation may respond more favorably to repeated exercises according to a direction of preference (what makes the symptoms decrease). The investigators do not know which of these two commonly-used treatments (manipulation or specific exercise) is better to treat low back pain.

详细描述

With the trends in health care focusing on treatment effectiveness, it is important for physical therapists to select the most appropriate intervention according to patient classification. Physical therapy interventions for management of LBP include therapeutic exercises and spinal manipulation.

The purpose of this study is to determine whether patients who fit the Clinical Prediction Rule (CPR) for spinal manipulation may respond instead to exercise according to repeated lumbar movements in the direction of preference.

The subjects for this study will be comprised of individuals referred for treatment of low back pain and data will be collected by physical therapists with certification in MDT who had experience treating patients through the use of spinal manipulation. Patient functional questionnaires and impairment measures will be used to analyze the patient's perceived level of function and outcome.

Following the completion of an informed consent, subjects will undergo a physical therapy examination by a licensed physical therapist. Patients will be included in the study if they meet the CPR for spinal manipulation as describe in earlier research 6,11. Following the examination, all qualified subjects will be randomly assigned to either the (1) spinal manipulation group or (2) the McKenzie (MDT) group and will receive treatment in accordance with their assigned group. The assessment tools administered at the initial examination will be readministered for follow-up analysis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
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

  • people who meet the clinical prediction rule for spinal manipulation

排除标准

  • people receiving worker's compensation
  • those who have had spinal surgery

结局指标

主要结局

Pain level as measured on numerical pain rating scale

时间窗: 1 year

次要结局

  • Oswestry score(1 year)

研究者

发起方
Daemen College
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ronald J. Schenk

Associate Professor Physical Therapy

Daemen College

研究点 (2)

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