Measurement of the Analgesic Efficacy of Shoulder Mobilization in Hemiplegic Patients
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 发起方
- 主要终点
- Pain evaluation with visual analogic scale
研究概览
简要总结
Hemiplegia is a high prevalence pathology with 1 per 1000 habitants in France. One of these complications is shoulder pain which affects about 35 to 70% of cases. The medical care of this complication is critical because it affects the patient's quality of life and also hinders participation in rehabilitation sessions slowing the recovery of independence in activities of daily living.
Literature confirmed the involvement of the scapula in the hemiplegic shoulder pain with his attitude pronounced lateral rotation. But no data to confirm that passive mobilization reduce shoulder pain.
Because no data available to permit us to determine the sample size we set-up this preliminary study to check if efficiency found in these preliminary data are consistent with an estimable real efficacy in a randomized trial feasible.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Hospitalized in Physical Medicine and Rehabilitation at Centre Hospitalier Universitaire Réunion (Site of Le Tampon)
- •Having made a cerebrovascular accident between 30 and 3 days before inclusion
- •with pain in the upper limb whose score with visual analogue scale is greater than or equal to 20 mm
- •able to understand the question: "Do you have arm pain?"
排除标准
- •with visual analogue scale score lower than 20 mm at the inclusion
- •with aphasia of comprehension
- •with medical contraindication for passive shoulder mobilisation (Shoulder fracture, dislocation,...)
- •opposing to any mobilization
- •with shoulder pathology previously known
- •history of cerebrovascular accident prior 30 days before inclusion
研究组 & 干预措施
Shoulder mobilisation
The shoulder mobilisation is performed daily by a physiotherapist for 45 days.
干预措施: Shoulder mobilisation (Procedure)
结局指标
主要结局
Pain evaluation with visual analogic scale
时间窗: Change of pain evaluation between Day 0 and Day 45
Proportion of patients reducing by at least 20 mm their score on the visual analogic scale (VAS) from baseline Day 45
次要结局
未报告次要终点