EFFECT OF MAITLAND AND MULLIGAN MOBILIZATION ON PAIN, RANGEOF MOTION AND FUNCTIONAL DISABILITY IN PATIENTS WITH ROTATORCUFF SYNDROME: RANDOMIZED CLINICAL TRIAL
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- 1. VAS
研究概览
简要总结
AIMS
The aim of this study is to find out the Effect of Maitland and Mulligan Mobilization on Pain, Range of Motion, and Functional Disability in patients with Rotator Cuff Syndrome: Randomized Clinical Trial
OBJECTIVES
• To evaluate the effect of Maitland mobilization on pain in individuals with Rotator Cuff Syndrome
• To evaluate the effect of Mulligan Mobilization on Pain, Range of Motion, and Functional Disability in Individuals with Rotator Cuff Syndrome
• To compare the effects of Maitland and Mulligan Mobilization in a patient with Rotator Cuff Syndrome.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 30.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Subjects having limited ROM of the shoulder joint
- •Partial rupture and suffering from Rotator cuff syndrome
- •No shoulder surgery
- •Willing to participate in the study.
排除标准
- •A recent myocardial infarction or major shoulder trauma
- •Patient with osteoporosis
- •Not willing to participate in the study
- •Tumours/malignancies/infections associated with the shoulder joint and upper limb metallic implants.
结局指标
主要结局
1. VAS
时间窗: Outcomes will be assessed at baseline and after | 6 weeks
3. DASH
时间窗: Outcomes will be assessed at baseline and after | 6 weeks
2. ROM
时间窗: Outcomes will be assessed at baseline and after | 6 weeks
次要结局
- 1. SF-36(Outcomes will be assessed at baseline and after)