The Impact of Mobilization With Movement on Pain, Function, and Quality of Life in Patients With Thoracic Outlet Syndrome: A Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- Changes in Pain Intensity
研究概览
简要总结
This randomized controlled trial aims to evaluate the effects of Mobilization with Movement (MWM) on pain, function, and quality of life in patients with Thoracic Outlet Syndrome (TOS) compared to conventional physiotherapy.
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 (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adults aged 18-65 years, diagnosed with TOS by a specialist, and experiencing symptoms for at least 3 months
排除标准
- •Previous surgery for TOS
- •contraindications to manual therapy
- •other comorbidities significantly affecting upper limb function
研究组 & 干预措施
Group A (experimental group)
MWM techniques combined with a tailored therapeutic exercise program
干预措施: Mobilization with Movement (MWM) and Tailored Therapeutic Exercise Program (Other)
Group B (control group)
Conventional physiotherapy combined with a tailored therapeutic exercise program
干预措施: Conventional Physiotherapy (Other)
结局指标
主要结局
Changes in Pain Intensity
时间窗: Changes in Pain intensity at Baseline, 4 weeks, 8 weeks, and 12 weeks (follow-up)
Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS).
次要结局
- Changes in Functional Status(Changes in Functional Status Baseline, 4 weeks, 8 weeks, and 12 weeks (follow-up))
- Changes in Cervical Range of Motion(Baseline, 4 weeks, 8 weeks, and 12 weeks (follow-up))
- Changes in Quality of Life(Changes in quality of life at Baseline, 4 weeks, 8 weeks, and 12 weeks (follow-up)aseline, 4 weeks, 8 weeks, and 12 weeks (follow-up))
研究者
Mohamed Magdy ElMeligie
Lecturer of Physical Therapy and Director of Electromyography Lab
Ahram Canadian University