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Effect of Sensorimotor Training on Pain and Gait Performance in Patients With Discogenic Sciatica

2026年9月1日 更新者:Yara Ahmed Mansour、Cairo University
This study aims to investigate the effect of sensorimotor training on gait performance in patients with discogenic sciatica.

研究概览

详细说明

Discogenic sciatica is commonly associated with pain, functional limitations, and alterations in gait performance resulting from nerve root involvement and impaired neuromuscular control. Sensorimotor training is an active rehabilitation approach that integrates sensory input with motor responses and may improve proprioception, postural control, balance, and movement coordination.

This study will investigate the additional effect of sensorimotor training in patients with chronic discogenic sciatica. Participants will receive a conventional physical therapy program consisting of interferential current therapy, hot packs, positioning according to directional preference, and static abdominal and back exercises. The experimental intervention will incorporate additional sensorimotor training, including proprioceptive neuromuscular facilitation (PNF)-based trunk exercises, balance training on unstable surfaces, colored-path sensorimotor exercises, and the Star Excursion Balance Exercise.

The sensorimotor program will use progressive task-specific exercises designed to challenge proprioception, balance, trunk control, and neuromuscular coordination. Exercise difficulty will be gradually progressed according to participants' abilities through changes in surface stability, movement complexity, reach distance, walking speed, and the incorporation of dual-task activities.

The study will evaluate changes in spatiotemporal gait parameters, pressure-pain threshold, and functional disability before and after the intervention. The findings may provide evidence regarding whether adding sensorimotor training to conventional physical therapy offers additional benefits for gait performance, pain-related outcomes, and functional ability in patients with chronic discogenic sciatica.

研究类型

介入性

注册 (估计的)

30

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

  • 姓名:Hend Mohammad Elsayed Ismail, PhD

学习地点

      • Gamasa、埃及
        • Outpatient clinic at the Faculty of Physical Therapy, Delta University
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  • Thirty patients of both sexes diagnosed with lumbar disc herniation affecting the L4-L5 and/or L5-S1 nerve roots will be included in this study.
  • Presence of lumbar disc herniation (LDH) will be confirmed by magnetic resonance imaging (MRI).
  • Age will range from 30 to 55 years.
  • Patients experiencing radiating pain along the sciatic nerve distribution (symptoms persisting for more than 3 months).
  • All patients must be employed in office-based jobs.
  • Berg Balance Scale score will range from 21 to 40 (moderate balance impairment).
  • Body Mass Index (BMI) will be within the normal to overweight range (18.5 29.9 kg/m²).
  • All the patients will be able to walk independently with or without minimal assistance.

Exclusion Criteria:

  • Patients with a history of spinal surgery will be excluded.
  • Presence of central neurological disorders (e.g., stroke).
  • Patients with other causes of low back pain which is not related to discogenic origin.
  • Affections of the musculoskeletal system including fractures.
  • Patients with severe balance impairment (Berg Balance Scale score < 21).
  • Presence of vestibular disorders or visual impairments affecting balance.
  • Patients are currently participating in other rehabilitation programs.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Standard physical therapy
Participants in this arm will receive a standard physical therapy program consisting of interferential current therapy, hot packs, positioning according to directional preference, and static abdominal and back exercises. The treatment will be administered three sessions per week for two months, with each session lasting approximately 45-60 minutes.
Standard physical therapy will include interferential current therapy applied over the lumbar region at 80-100 Hz for 15-20 minutes, hot packs applied over the lumbar paraspinal region for 10 minutes, positioning according to the patient's directional preference for 10 minutes or as tolerated, and static abdominal and back exercises targeting the transversus abdominis and multifidus. The exercises will be performed as 3 sets of 10 repetitions, with each contraction held for 10 seconds followed by 5 seconds of rest.
实验性的:Sensorimotor Training Plus Standard Physical Therapy
Participants in this arm will receive the same standard physical therapy program administered to the active comparator arm, in addition to a sensorimotor training program. The sensorimotor training will include PNF-based trunk exercises, balance training on unstable surfaces, colored-path sensorimotor exercises, and the Star Excursion Balance Exercise. The treatment will be administered three sessions per week for two months, with each session lasting approximately 45-60 minutes.
Standard physical therapy will include interferential current therapy applied over the lumbar region at 80-100 Hz for 15-20 minutes, hot packs applied over the lumbar paraspinal region for 10 minutes, positioning according to the patient's directional preference for 10 minutes or as tolerated, and static abdominal and back exercises targeting the transversus abdominis and multifidus. The exercises will be performed as 3 sets of 10 repetitions, with each contraction held for 10 seconds followed by 5 seconds of rest.
Sensorimotor training will include PNF-based trunk exercises, balance training on unstable surfaces, colored-path sensorimotor exercises, and the Star Excursion Balance Exercise. The program will incorporate progressive challenges to trunk control, balance, proprioception, and neuromuscular coordination. Progression will include unstable surfaces, alternating limb movements, single-leg and cross bridging, increased walking speed, dual-task activities, increased reach distance, and increased exercise complexity according to patient tolerance.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Walking Speed
大体时间:2 months
Walking speed will be assessed using the FreeMed® baropodometric platform with FREESTEP software and reported in meters per second (m/s).
2 months
Stride Length
大体时间:2 months
Stride length will be assessed using the FreeMed® baropodometric platform with FREESTEP software and reported in millimeters (mm).
2 months
Cadence
大体时间:2 months
Cadence will be assessed using the FreeMed® baropodometric platform with FREESTEP software and reported as steps per minute (steps/min).
2 months
Stance Time
大体时间:2 months
Stance time will be assessed using the FreeMed® baropodometric platform with FREESTEP software and reported in seconds (s).
2 months

次要结果测量

结果测量
措施说明
大体时间
Pressure-Pain Threshold
大体时间:2 months
Pressure-pain threshold will be assessed using a pressure algometer at the lumbar paraspinal, gluteus medius, and piriformis muscles. Higher values indicate greater pressure-pain tolerance.
2 months
Functional Disability
大体时间:2 months
Functional disability will be assessed using the Oswestry Disability Index (ODI). The score will be expressed as a percentage from 0% to 100%, with higher scores indicating greater disability.
2 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 学习椅:Moshera Hassan Darwiesh, PhD、Professor, Cairo University
  • 研究主任:Omar Mohamed Said, PhD、Lecturer, Cairo University
  • 研究主任:Hend Mohammad Elsayed Ismail, PhD、Lecturer, Delta University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月7日

初级完成 (估计的)

2027年1月7日

研究完成 (估计的)

2027年1月21日

研究注册日期

首次提交

2026年9月1日

首先提交符合 QC 标准的

2026年9月1日

首次发布 (实际的)

2026年9月4日

研究记录更新

最后更新发布 (实际的)

2026年9月4日

上次提交的符合 QC 标准的更新

2026年9月1日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • F.PT. 2607107

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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