Effects of Decompression on Pain, Range of Motion and Function in Patient With Acute vs Chronic Lumbar Radiculopathy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Visual Analogue Scale
研究概览
简要总结
The study will be done to evaluate the effectiveness of Lumbar Spinal Decompression in patients with acute vs chronic lumbar radiculopathy. Study design will be Randomized control trial and sample size will be 30. Duration of study was of 6 month, convenient sampling was done. Data will be collected from DHQ Daska were randomly allocated in three groups via lottery method, baseline assessment was done. Patients of both gender (male and female) from 18 to 50 years with lumbar radiculopathy diagnosed through X-ray and physical examination will be included. Patients with systemic soft tissue and bony diseases will be excluded. Intervention duration of 4 weeks, 3 sessions in a week. Decompression of lumbar spine will be given once in a week. Whole procedure of treatment program will given to patients and written informed consent will be taken. Basic tools will be Visual analog scale (VAS), SLR, ODI, Inclinometer. Data was analyzed by using SPSS version 21
详细描述
Low back pain (LBP) is one of the most common musculoskeletal conditions treated by physical therapists. Although lumbar traction is frequently used by physical therapists in the treatment of patients with LBP. We will use Manual Lumber Spinal Traction on patients with acute vs chronic lumber radiculopathy. The current study will determine the effect of decompression in relieving pain, increase range of motion and improving function in patients of acute and chronic lumbar radiculopathy. Lumbar traction (LT) is routinely used on its own or in conjunction with other treatments for the management of lumbar sciatica. We will use Manual lumbar traction along with hot pack, tens, mobilization and exercise therapy. Intervention duration of 4 weeks, 3 sessions in a week. Decompression of lumbar spine will be given once in a week.
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 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •history of radicular pain with straight leg raise (SLR).
- •Patients in the acute phase of (up to 6 weeks) included in group A
- •Patients in chronic phase of (more than 6 weeks) included in group B
排除标准
- •Any systemic soft tissue and bony disease.
- •Patient with spinal tuberculosis, spinal fractures, pregnancy, cancer.
- •Any recent surgery.
- •Patient with any cervical or thoracic problem.
- •Patients with any other serious pathology/red flags
研究组 & 干预措施
Group A
Decompression + Hot pack, TENS, Mobilization, Exercise Therapy
干预措施: Decompression + Hot pack, TENS, Mobilization, Exercise Therapy (Other)
Group B
Decompression + Hot pack, TENS, Mobilization, Exercise Therapy
干预措施: Decompression + Hot pack , TENS , Mobilization , Exercise Therapy (Other)
Group C
Hot pack , TENS, Mobilization, Exercise therapy
干预措施: Hot pack , TENS, Mobilization, Exercise therapy (Other)
结局指标
主要结局
Visual Analogue Scale
时间窗: 4th week
A Visual Analogue Scale (VAS) is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured
次要结局
- MODIFIED OSWESTRY LOW BACK PAIN DISABILITY QUESTIONNAIRE(4th Week)