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临床试验/NCT06212011
NCT06212011已完成不适用

Investigation on the Effect of Functional Neuromuscular Electrical Stimulation Technique Applied to the Lumbar Multifidus Muscle On Body Kinetics and Kinematics During Sit to Stand Activity In Individuals With Nonspecific Low Back Pain

Hacettepe University2 个研究点 分布在 2 个国家目标入组 24 人开始时间: 2024年5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
入组人数
24
试验地点
2
主要终点
Changes in ground reaction force during sit-to-stand activity

研究概览

简要总结

The goal of this randomized controlled trial, is to investigate the effect of functional NMES and conventional NMES applied to the lumbar multifidus muscle on body kinematic and kinetic values during the sit-to-stand in individuals with non-specific low back pain. Our study will include 24 participants between the ages of 18-65. Which physiotherapy intervention will be applied to the participants will be determined by the block randomization method, using a table of random numbers. After randomization; NMES to the participants' lumbar multifidus muscle during physiotherapy intervention will be applied in two groups; In the first group, NMES will be applied with the conventional technique during prone position and in the second group, NMES will be applied with the functional technique during the sit-to-stand activity. Evaluations will be made twice for each participant- before and after the intervention. During the evaluation, data regarding the change in body kinetics and kinematics of individuals during the sit-to-stand activity will be recorded with a Vicon camera system. For secondary outcome measures, a visual analog scale will be used to evaluate pain, the Roland Morris Disability Questionnaire and the Oswestry Disability Index will be used to evaluate functional status, and the Tampa Kinesiophobia Scale will be used to evaluate fear-avoidance behavior.

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
None

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

  • History of chronic low back pain (12 weeks<)
  • Pain in the lumbar and/or hip area (VAS>3)
  • Volunteering to participate in the study

排除标准

  • History of neurological, metabolic, cardiovascular disease
  • Having had spinal surgery, specific lumbar pathology, scoliosis, pregnancy, history of systemic or degenerative disease
  • Musculoskeletal system pathology in the last year
  • Body mass index being over 30 kg/m2
  • Continuing any exercise program

研究组 & 干预措施

Functional Neuromuscular Electrical Stimulation Group

Experimental

Functional NMES involves stimulating the lumbar multifidus muscle while the individual performs a sit-to-stand activity.

干预措施: Functional Neuromuscular Electrical Stimulation (Other)

Conventional Neuromuscular Electrical Stimulation Group

Experimental

Conventional NMES intervention involves only stimulating the lumbar multifidus muscle while the individual is in the prone position, and the individual will not reveal any voluntary contraction during stimulation.

干预措施: Conventional Neuromuscular Electrical Stimulation (Other)

结局指标

主要结局

Changes in ground reaction force during sit-to-stand activity

时间窗: Baseline and first week after 8-week intervention

Ground reaction force will be evaluated using force plates (2xAMTI force plates).

Changes in kinematics of the Lumbar Spine and Hip During sit-to-stand activity

时间窗: Baseline and first week after 8-week intervention

With kinematic analysis, the mean, minimum and maximum range of motion of the lumbar spine and hip joint during the sit-to-stand activity will be evaluated and recorded in degrees using the vicon motion capture system (Vicon, 6xVantage 5 Cameras 5MP@420FPS, 2xVue Video Cameras).

次要结局

  • Hip and Lumbar spine range of motion(Baseline and first week after 8-week intervention)
  • Shortness of the hip flexor, knee flexor and plantar flexor muscles(Baseline and first week after 8-week intervention)
  • Beighton test(Baseline and first week after 8-week intervention)
  • Visual analogue scale(Baseline and first week after 8-week intervention)
  • Oswestry Disability Index(Baseline and first week after 8-week intervention)
  • Roland-Morris Disability Questionnaire(Baseline and first week after 8-week intervention)
  • Tampa Kinesiophobia Scale(Baseline and first week after 8-week intervention)

研究者

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

Duygu Yilmaz

Principal Investigator

Hacettepe University

研究点 (2)

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