NCT01529398已完成2 期
Efficacy of a Sensorimotor Training in Patients With Knee Osteoarthritis: a Randomized Clinical Trial
Federal University of São Paulo2 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2008年3月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 96
- 试验地点
- 2
- 主要终点
- Visual analogue scale of pain (VAS)
研究概览
简要总结
People with knee osteoarthritis (OA) have functional instability and defective neuromuscular function, it was recently suggested that sensorimotor exercises may be important and needed to improve the effectiveness of training programs for these patients. This study objective was to compare the effectiveness of a supervised resistance muscular training (RT) versus sensorimotor training (SMT) for patients with Knee OA, on decrease of pain and functional improvement.
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
- 50 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients diagnosed with tibiofemoral osteoarthritis;
- •Both genders;
- •Age> 50 years <75 years;
- •Completion of clinical and radiological criteria of the American College of Rheumatology (ACR) criteria for knee OA;
- •No physical activity in the previous 3 months;
- •Education level from the 4th grade of primary school.
排除标准
- •uncontrolled hypertension;
- •decompensated diabetes mellitus;
- •uncontrolled thyroid diseases;
- •cardiorespiratory disease (ischemia, arrhythmia, chest pain, or exercise-induced bronchospasm), liver abnormalities;
- •Patients with grade IV functional limitation that needed devices to walk(Kellgren-Lawrence radiographic classification);
- •Patients in a period of sick leave by the INSS or any other related factor;
- •Other rheumatic diseases.
研究组 & 干预措施
Control group (CG)
Sham Comparator
干预措施: Control group (CG) (Other)
sensorimotor training (SMT)
Active Comparator
干预措施: Sensorimotor training (SMT) (Other)
Resistance training (RT)
Active Comparator
干预措施: Resistance training (RT) (Other)
结局指标
主要结局
Visual analogue scale of pain (VAS)
时间窗: 16 weeks
Get Up and Go Test
时间窗: 16 weeks
次要结局
- Tinetti Test(16 weeks)
- Medical Outcomes Study Short Form (SF-36)(16 weeks)
- Berg Balance Test(16 weeks)
- electromyographic analysis of quadriceps muscle (EMG)(16 weeks)
- Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)(16 weeks)
- isometric quadriceps strength(16 weeks)
- activities of daily living scale (ADLS)(16 weeks)
研究者
Aline Basolli Gomiero
Physical Therapist
Federal University of São Paulo
研究点 (2)
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