A Randomized Comparative Study to Evaluate the Efficacy of Sustained Natural Apophyseal Glide Versus Mulligans Bent Leg Raise Technique Along With Traditional Physiotherapy in Patients With Non Specific Mechanical Low Back Pain
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 58
- 试验地点
- 1
- 主要终点
- NPRS -Numeric Pain Rating Scale
研究概览
简要总结
This randomized comparative experimental study aims to evaluate and compare the effectiveness of two manual therapy techniques Sustained Natural Apophyseal Glide SNAG and Mulligans Bent Leg Raise BLR when used alongside traditional physiotherapy in the treatment of non specific mechanical low back pain NSMLBP. A total of 58 participants aged 18 to 60 years will be randomly assigned into two equal groups. Group A will receive SNAG with traditional physiotherapy while Group B will receive Mulligans BLR technique with traditional physiotherapy. Both groups will undergo treatment three times per week for four weeks. Outcome measures including pain measured by Numeric Pain Rating Scale NPRS functional disability assessed by Oswestry Disability Index ODI lumbar range of motion measured by goniometry and the Straight Leg Raise SLR test will be assessed at baseline mid intervention second week and post intervention fourth week. The study seeks to determine which manual therapy approach provides superior clinical outcomes in pain relief mobility and functional improvement in patients with NSMLBP.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- All
入选标准
- •Both males and females Patients with non-specific Mechanical low back pain.
排除标准
- •1.Fracture 2.Tumors 3.Infection 4.Inflammatory diseases 5.Individuals with neurological deficits 6.Chronic pathological pain 7.Conditions that could affect their ability to participate in the exercises.
- •8.Patients who had undergone previous surgical interventions for low back pain.
- •9.Any contraindication to physiotherapy & manual therapy.
- •10.Those who were currently receiving other forms of treatment for low back pain that could confound the results.
结局指标
主要结局
NPRS -Numeric Pain Rating Scale
时间窗: Baseline (Day 0) | Mid-intervention (on 15th day) | post intervention (on 30th day)
ODI-Oswestry Disability Index
时间窗: Baseline (Day 0) | Mid-intervention (on 15th day) | post intervention (on 30th day)
GONIOMETER
时间窗: Baseline (Day 0) | Mid-intervention (on 15th day) | post intervention (on 30th day)
Straight Leg Raise (SLR) test
时间窗: Baseline (Day 0) | Mid-intervention (on 15th day) | post intervention (on 30th day)
次要结局
未报告次要终点
