Effec of Maitland in Shoulder Pathology
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 63
- 试验地点
- 2
- 主要终点
- Change of Visual Analog Scale (VAS)
研究概览
简要总结
The shoulder is a mobile structure which generates a lot of pathologies. One of them is rotator cuff tendinosis. On the other hand, it has been investigated that Maitland is effective for reducing pain and for mobility in the cervical and lumbar spine and in joints such as the knee and ankle, however, there are few studies that confirm that it is effective in shoulder pathologies.So here the investigatprs want to study the effectiveness of Maitland as an adjunctive treatment for shoulder pathologies, comparing it with conventional physiotherapy treatment, in relation to the reduction of pain and increased mobility. For that the investigators have a randomized clinical trial with two group.
详细描述
Group 1 receives tens, SW, conventional physiotherapy and exercises as treatment. Group 2 receives tens, SW, Mailtland, and exercises. An assessment is carried out at the beginning of the treatment, at the end and 2-4 weeks after finishing the treatment. The EVA ASES, DASH and SF-36 scales are included and the biomechanics study is used for the range of mobility.
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
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Have a shoulder pathology.
- •Have a restriction at least of two ranges of movement of the shoulder.
- •Sign the consent before starting the study.
排除标准
- •Patients with a history of shoulder or neck surgery.
- •Patients with neurological damage such as stroke or disease of Parkinson's, as well as those with rheumatism, osteoporosis, surgical fixation, or malignant tumors.
- •Have a radiating pain in shoulder from a cervical injury.
- •Pregnant patients.
- •Patients who do not sign the consent before starting the study.
结局指标
主要结局
Change of Visual Analog Scale (VAS)
时间窗: Baseline and 1, 5, and 7 weeks after treatment
Visual analogue score (VAS) was done at rest and at shoulder movement. VAS was explained to the patients during assessment as 0 equal no pain and 10 equal worst imaginable pain.
Change of Disabilities of the Arm, Shoulder and Hand (DASH)
时间窗: Baseline and 1, 5, and 7 weeks after treatment
Disabilities of the Arm, Shoulder and Hand (DASH) was filled by patient during assessment as 0 equal better functionality and 100 equal worst functionality
Change of Range of Motion (ROM)
时间窗: Baseline and 1, 5, and 7 weeks after treatment
Active ROM of the affected shoulder is measured using a Mechanic Analysis to assess range of motion. These measurements included abduction, flexion, internal rotation, and external rotation.
次要结局
- Change of American shoulder and elbow Surgeons" (ASES)(Baseline and 1, 5, and 7 weeks after treatment)
- Change of 36-Item Health Survey (SF-36)(Baseline and 1, 5, and 7 weeks after treatment)
研究者
Karishma Chuhermal Lalwani Mangtani
Principal Investigator
University of Las Palmas de Gran Canaria