Feasibility of Modified Constraint-induced Movement Therapy Combined With Visual-spatial Cueing Strategy in Patients With Acute Stroke
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 8
- 试验地点
- 2
- 主要终点
- Number of tasks realized per protocol between the two arms
研究概览
简要总结
The aim of this study is to test the feasibility of a constraint intervention combined with visual-spatial cueing strategy in patients with acute stroke to improve their daily life activities.
详细描述
As part of treatment in acute stroke (from D0 to D14), the investigators were able to observe that despite motor recovery during physiotherapy sessions, it remained difficult for some patients to use their affected arm (AA) during activities of daily life (ADL). This mechanism of "learned non-use" would be due to a cognitive process decreasing the use of the AA and could partly explain that 75% of patients maintain an upper limb deficit at 3-6 month post-stroke.
In order to combat this phenomenon, a bottom up method (sensorimotor action on the deficit) of constraint-induced movement therapy (CIMT) has been developed and consists in immobilizing the unaffected arm to force the use of the AA.
This technique has proved its effectiveness in the chronic phase and has also recently been proven to improve motor performance in the acute phase. Transposing progress on ADL, however, remains difficult because CIMT does not contain adequate behavioral strategies.
To help the patient mobilize these strategies, coupling of CIMT with a top-down method (conscious action on motor skills) has been successfully tested as an intervention of an occupational therapist with the patient at least 1h / day. This intervention remains not compatible with the investigators care organization because the caregiver can not spend that amount of time with each patient.
Investigators therefore propose to associate CIMT with another top down technique: visual-spatial cueing (use of panels and/or visual messages to encourage the conscious use of the AA) and investigators want to evaluate the effectiveness of this treatment on learning transfer to ADL.
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
- 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
- •Hospitalized patient in neurovascular unit for stroke
- •Time since stroke between 2 and 4 days
- •Movement capacity of the upper arm (against gravity) :
- •Ability to extend actively the metacarpophalangeal and interphalangeal joints at least 10°, and the wrist 20°
- •Ability to bend actively the elbow at least 45°
- •Ability to bend and abduct actively the shoulder at least ≥ 45°
- •Age ≥ 18 years old
- •Patient agreement to join the study
- •Patient covered by french social security
排除标准
- •Excessive spasticity : score > 2 on the modified Ashworth scale
- •Excessive pain in the affected arm : score ≥ 4 on the visual analogue scale
- •Joint limitation on the affected arm
- •Patient under guardianship or curatorship
- •Pregnant or breastfeeding woman
结局指标
主要结局
Number of tasks realized per protocol between the two arms
时间窗: Day 15
Variances to a predetermined checklist
次要结局
- Arm motor function(Day 0, Day 15 and Month 3)
- Anxiety and Depression evolution(Day 0, Day 7, Day 15 and Month 3)
- Situation of patient after neurovascular unit(Month 3)
- Pain evolution(Day 0, Day 7, Day 15 and Month 3)