Efficacy of Mulligan Mobilization Technique in Chronic Non-Spesific Low Back Pain
试验速览
- 阶段
- 不适用
- 入组人数
- 55
- 试验地点
- 2
- 主要终点
- Change of Range of Motion from baseline at 3 weeks and from baseline at 6 months
研究概览
简要总结
Fifty five participants diagnosed with CNSLBP, will randomized into three groups. Group I (18 subjects) will receive 15 sessions of Conventional Physiotherapy program (CPP) 5 times per week, Group II (19 subjects) will receive 9 sessions of SNAGs, and Group III will receive CPP plus SNAGs. Outcome measures are pain, ROM, spinal mobility, fear avoidance behaviour and function. Measurements will record before, after and 6 month after the end of the treatment.
详细描述
Inclussion criterias are; low back pain for at least 3 months, intensity of pain ranges from 3 to 6 according to VAS. Exclussion criterias are; undergoing surgical operation in the lumbar region or having a surgical indication, having an exercise therapy and / or physical therapy in the last 1 year, a history of trauma involving lumbar region and systemic and inflammatory disease targeting this region, participants using corticosteroids for a long time and being pregnant.Acording to our criterias 55 participants diagnosed with CNSLBP will randomised into three groups. Group 1 will receive Conventional Physiotherapy programme consisting of Hot pack, US and TENS applications. Group II aill receive Lumbar SNAGS consisting of Lumbar Extension SNAGS in prone, SNAGS in lion position and Lumbar flexion SNAGS in sitting, techniques. Group III will receive 9 sessions of SNAGs, and Group III will receive CPP plus SNAGs.Outcome measures are pain, ROM, spinal mobility, fear avoidance behaviour and function. Measurements will record before, after and 6 month after the end of the treatment. All treatment groups were treated with the same researcher. All assessments were made by another blind researcher three times at before, after and 6 month after treatment.
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
- Single (Investigator)
盲法说明
All assessments were made by another blind researcher three times at before, after and 6 month after treatment.
入排标准
- 年龄范围
- 20 Years 至 50 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •low back pain for at least 3 months
- •intensity of pain ranges from 3 to 6 according to VAS
排除标准
- •undergoing surgical operation in the lumbar region or having a surgical indication having an exercise therapy and / or physical therapy in the last 1 year
- •a history of trauma involving lumbar region and systemic and inflammatory disease targeting this region
- •corticosteroids consumption for a long time
- •being pregnant.
结局指标
主要结局
Change of Range of Motion from baseline at 3 weeks and from baseline at 6 months
时间窗: Baseline, 3 weeks,6 months
ROM is measured by BROM II device during flexion and extension activity.
Change from Pain Intensity from baseline at 3 weeks and from baseline at 6 months
时间窗: Baseline, 3 weeks,6 months
Pain intensity during flexion and extension activity in lumbar region is measured by Numeric pain scale in which "0" shows No pain while "10" shows worst pain.
Change of Spinal Mobility from baseline at 3 weeks and from baseline at 6 months
时间窗: Baseline, 3 weeks,6 months
Spinal mobility measured by Schober test.
次要结局
- Change from Fear Avoidance Behaviour from baseline at 3 weeks and from baseline at 6 months(Baseline, 3 weeks,6 months)
- Change from Disability level from baseline at 3 weeks and from baseline at 6 months(Baseline, 3 weeks,6 months)