Comparison of Dry Needling and Dry Cupping in Positional Fault of Pelvis Due to Myofascial Trigger Points in Quadratus Lumborum
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 26
- 试验地点
- 2
- 主要终点
- Change in Range of Motion of lumbar spine side flexion by 'Goniometer'
研究概览
简要总结
This project was a Randomized clinical trial conducted to Compare the effects of dry needling and dry cupping in Positional fault of pelvis due to Myofascial trigger points in Quadratus Lumborum so that we can have best treatment option for patients with myofascial trigger points.
详细描述
Non Probability Convenient sampling was done. Patients following eligibility criteria from Physiotherapy department of Islam Central hospital, Sialkot were considered. Sample size was calculated with Epitool calculator. 26 Participants were randomly allocated in two groups equally via convenient sampling method. Baseline assessment was done initially. Group A was given Dry needling technique and Group B was given Dry Cupping along with conventional physiotherapy treatment (hot pack and stretching). Duration of research was almost 6 months. Participants were treated 6 times over a 3 week period with 2 treatment sessions per week per patient. Pre and Post treatment readings were taken in 1st and 6th session over a 3 week period respectively. A follow up reading was also taken after 1 month for checking prolonged post treatment effects. Assessment was done via Pressure pain threshold Scale, Pelvic goniometer and Measuring tape for assessing functional positional fault of pelvis and muscle length of Quadratus Lumborum. All participants were provided written informed consent prior to commencement of the procedures. They were free to quit the treatment at any stage of research. Data was analyzed by using SPSS version 23.
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 (Participant)
入排标准
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •On palpation the presence of at least 1 active trigger point in quadratus lumborum. So the patient presents with low back pain.
- •Patients presents with positional fault of pelvis (lateral tilt)(4).
- •Patients having chronic Low Back Pain for at least more than 6 months(3).
- •Patients agree to get treatment sessions for the research work.
排除标准
- •Participants should not have taken any medications like analgesics, anti-coagulants, Non-steroidal anti-inflammatory drugs or muscle relaxants during this study or even 3 days before this study.
- •Participants should not have received any other treatment for the pain management, because it will affect the results of the study.
- •Patients with bleeding disorders, local or systemic infection, acute muscle trauma.
- •Patients with comorbid conditions.
- •Patients with severe physical disability and true leg length discrepancy(1).
- •Pregnant females
结局指标
主要结局
Change in Range of Motion of lumbar spine side flexion by 'Goniometer'
时间窗: Baseline, 6th session(at 3rd week), follow up session after 1 month
Change in ROM from baseline was measured at 6th session. A follow up reading was taken after 1 month for checking prolonged post treatment effects. A goniometer is a device that measures an angle or permits rotation of an object to a definite position
Change in Pain by 'Pressure Pain Algometer'
时间窗: Baseline, 6th session(at 3rd week), follow up session after 1 month
Change in Pain from baseline was checked at 6th session by Pressure Pain Algometer. A follow up reading was also taken after 1 month for checking prolonged post treatment effects.
次要结局
- Change in pain by 'Numeric Pain Rating Scale'(Baseline, 6th session(at 3rd week), follow up session after 1 month)
- Change in Range of Motion of lumbar side flexion by Measuring tape(Baseline, 6th session(at 3rd week), follow up session after 1 month)