Integrated Neuromuscular Inhibition Technique Versus Instrument Assisted Soft Tissue Mobilization in Patients With Chronic Non Specific Low Back Pain
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 45
- 主要终点
- change in lumber proprioception
研究概览
简要总结
this study will be conducted to identify the difference between the effect of integrated neuromuscular inhibition technique and instrument assisted soft tissue mobilization on back pain, pain threshold, back rang of motion ,back proprioception and back disability in chronic non specific low back pain
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 (Participant, Outcomes Assessor)
盲法说明
Double ( participant ,outcomes assessor)
入排标准
- 年龄范围
- 18 Years 至 30 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •The patient's age ranged from 18 to 30 years.(Geogre et al, 2021)
- •Patients with low back pain for more than 3 months (pain felt between T12 and the gluteal fold).
- •Patient with chronic low back pain
- •Normal body mass index from 18 -25kg/m2.
排除标准
- •The subjects will be excluded if they have any of the followings:
- •Lumbar discogenic lesions or any inflammatory arthritis, tumors, infection involving the lumbar spine.
- •Patients with decreased range of motion secondary to congenital anomalies, muscular contracture, or bony block.
- •Previous lumbar or hip surgery or trauma.
- •Any hip structural abnormality such as malformations, impingements and degeneration.
- •Patients With cognitive impairments that would limit their participation
研究组 & 干预措施
Group A: integrated neuromuscular inhibition technique
Group A: patient will receive integrated neuromuscular inhibition technique and conventional physical therapy program for 3 sessions /week over 4 weeks periods
干预措施: Experimental: Group A: integrated neuromuscular inhibition technique (Other)
Group B :Instrument assissted soft tissue mobilization
Group B : patient will receive Instrument assissted soft tissue mobilization technique and conventional physical therapy program for 3 sessions /week over 4 weeks periods
干预措施: Experimental: Group B :Instrument assissted soft tissue mobilization (Other)
Group C:conventional physical therapy
Group C: patient will receive conventional physical therapy only in the form of ( stretch for hamstring ,illiopoaps ,low back muscle and strenghtning for abdominal ,back muscles and side support exercise and quadriped exercise)
干预措施: control group C conventional physical therapy (Other)
结局指标
主要结局
change in lumber proprioception
时间窗: Evaluation will be performed priod to the first treatment session :as a baseline measure,and at least treatment session (after 4 weeks)as a post-treatment measure
change in lumbar proprioception will be measured by dual inclinometer for 3 group pre-and post-treatment
chang in pain pressure threshold
时间窗: Evaluation will be performed priod to the first treatment session :as a baseline measure,and at least treatment session (after 4 weeks)as a post-treatment measure
change in lower back pain threshold will be measured by pressure algometer for 3 group pre-and post-treatment
次要结局
- chang in lumbar rang of motion(ROM)(Evaluation will be performed priod to the first treatment session :as a baseline measure,and at least treatment session (after 4 weeks)as a post-treatment measure)
- functional disability oFlumbar spine(Evaluation will be performed priod to the first treatment session :as a baseline measure,and at least treatment session (after 4 weeks)as a post-treatment measure)
- pain level of lumbar spine(Evaluation will be performed priod to the first treatment session :as a baseline measure,and at least treatment session (after 4 weeks)as a post-treatment measure)
研究者
Heba Salama Mansour Mousa
Principal investigator
Cairo University