NCT03856983已完成不适用
Benefits of Observing Point-light Displays in Postoperative Rehabilitation of the Total Knee Prosthesis.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 36
- 试验地点
- 1
- 主要终点
- Compare the evaluation of the point light display relative to conventional rehabilitation
研究概览
简要总结
The LOARAL project concerns patients who have undergone total knee arthroplasty to treat symptomatic osteoarthritis. Patient will be divided into two groups: a control group where patients will do standard rehabilitation and an experimental group where patients will do standard rehabilitation associated with the judgement of point-light display. The aim of this study is to validate the use of point-light display for the Rehabilitation of patients with a totalarthroplasty of the knee.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
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
- •Volunteers over 18 years of age who have undergone knee surgery
排除标准
- •Any locomotor condition not due to knee surgery
- •Uncorrected visual disturbances
- •Comorbidity altering locomotion (history of stroke, neurological condition, inflammatory rheumatism)
结局指标
主要结局
Compare the evaluation of the point light display relative to conventional rehabilitation
时间窗: Rehabilitation during 3 weeks
The time to realize the time up and go test will be assessed at inclusion and at the end of the program.
次要结局
- Compare the evaluation of the point light display on functional recovery(At the end of the program (3 weeks max))
- Compare the evaluation of the point light display on the detection and action recognition(At the end of the program (3 weeks max))
- Compare the evaluation of the point light display on the feeling of self-efficacy personal(At the end of the program (3 weeks max))
研究者
研究点 (1)
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