跳至主要内容
临床试验/CTRI/2024/06/069282
CTRI/2024/06/069282尚未招募1 期

To assess the clinical and functional outcomes following conservative management of mechanical low back pain with active structured rehabilitation program using spine biofeedback device

Armed Forces Medical College1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年7月30日最近更新:

试验速览

阶段
1 期
状态
尚未招募
入组人数
40
试验地点
1
主要终点
Pain severity as per VAS score

研究概览

简要总结

A quasi experimental study to assess the clinical and functional outcomes in forms of pain, disability, ROM and strength of trunk muscle, before and after spine rehabilitation using spine biofeedback device with an aim to check the efficacy of device in sub-acute and chronic low back patient

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • Subacute and chronic mechanical low back pain.

排除标准

  • Pregnancy, Vertebral compression fracture, severe progressive neurologic deficit including cauda equina syndrome, spinal infection, spinal neoplasm, inflammatory spondyloarthritis, previous spine surgery and unwillingness due to any reason.

结局指标

主要结局

Pain severity as per VAS score

时间窗: At baseline and 12 weeks post rehabilitation

Disability as per ODI

时间窗: At baseline and 12 weeks post rehabilitation

Trunk range of motion and strength

时间窗: At baseline and 12 weeks post rehabilitation

次要结局

  • Isolated trunk ROM & strength in patients with mechanical low back pain on first visit & comparison with normal ROM & strength in normal adults(Baseline at first visit)

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Amir Khan

Armed Forces Medical College

研究点 (1)

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