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首页> 外文期刊>BMC Pediatrics >Minimising impairment : Protocol for a multicentre randomised controlled trial of upper limb orthoses for children with cerebral palsy
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Minimising impairment : Protocol for a multicentre randomised controlled trial of upper limb orthoses for children with cerebral palsy

机译:最小化损伤:针对脑瘫儿童的上肢矫形器多中心随机对照试验的方案

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Background Upper limb orthoses are frequently prescribed for children with cerebral palsy (CP) who have muscle overactivity predominantly due to spasticity, with little evidence of long-term effectiveness. Clinical consensus is that orthoses help to preserve range of movement: nevertheless, they can be complex to construct, expensive, uncomfortable and require commitment from parents and children to wear. This protocol paper describes a randomised controlled trial to evaluate whether long-term use of rigid wrist/hand orthoses (WHO) in children with CP, combined with usual multidisciplinary care, can prevent or reduce musculoskeletal impairments, including muscle stiffness/tone and loss of movement range, compared to usual multidisciplinary care alone. Methods/design This pragmatic, multicentre, assessor-blinded randomised controlled trial with economic analysis will recruit 194 children with CP, aged 5–15 years, who present with flexor muscle stiffness of the wrist and/or fingers/thumb (Modified Ashworth Scale score ≥1). Children, recruited from treatment centres in Victoria, New South Wales and Western Australia, will be randomised to groups (1:1 allocation) using concealed procedures. All children will receive care typically provided by their treating organisation. The treatment group will receive a custom-made serially adjustable rigid WHO, prescribed for 6?h nightly (or daily) to wear for 3?years. An application developed for mobile devices will monitor WHO wearing time and adverse events. The control group will not receive a WHO, and will cease wearing one if previously prescribed. Outcomes will be measured 6 monthly over a period of 3?years. The primary outcome is passive range of wrist extension, measured with fingers extended using a goniometer at 3?years. Secondary outcomes include muscle stiffness, spasticity, pain, grip strength and hand deformity. Activity, participation, quality of life, cost and cost-effectiveness will also be assessed. Discussion This study will provide evidence to inform clinicians, services, funding agencies and parents/carers of children with CP whether the provision of a rigid WHO to reduce upper limb impairment, in combination with usual multidisciplinary care, is worth the effort and costs. Trial registration ANZ Clinical Trials Registry: U1111-1164-0572 .
机译:背景技术上肢矫形器通常用于脑瘫(CP)的儿童,这些儿童主要由于痉挛而肌肉过度活动,几乎没有长期有效的证据。临床共识是,矫形器有助于保持活动范围:尽管如此,矫形器的构造复杂,昂贵,不舒适,并且需要父母和孩子的穿戴。该方案文件描述了一项随机对照试验,以评估CP患儿长期使用刚性手腕/手矫形器(WHO)并结合常规的多学科护理能否预防或减少肌肉骨骼损伤,包括肌肉僵硬/音调和肌力丧失。与常规的多学科护理相比,其运动范围更大。方法/设计该实用,多中心,评估人盲的经济分析随机对照试验将招募194名5至15岁的CP儿童,他们表现出手腕和/或手指/拇指的屈肌僵硬(改良的Ashworth量表评分≥1)。从维多利亚,新南威尔士州和西澳大利亚州的治疗中心招募的儿童将采用隐蔽程序随机分组(按1:1分配)。所有儿童通常都会得到其治疗机构提供的照顾。治疗组将接受定制的可连续调整的刚性WHO,按规定,每晚(或每天)每天6小时,佩戴3年。为移动设备开发的应用程序将监视WHO的佩戴时间和不良事件。对照组将不会接受世界卫生组织,并且如果先前有规定,将不再佩戴该组织。结果将在3年内每月6次进行评估。主要结果是腕部伸展的被动范围,用测角计在3年时用手指伸展来测量。次要结果包括肌肉僵硬,痉挛,疼痛,握力和手部畸形。活动,参与,生活质量,成本和成本效益也将得到评估。讨论这项研究将提供证据,以告知临床医生,服务机构,资助机构以及患有CP的儿童家长/照护者,与常规的多学科护理相结合,提供严格的WHO减少上肢损伤的措施是否值得付出努力和成本。试验注册ANZ临床试验注册:U1111-1164-0572。

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