首页> 外文期刊>BMC Neurology >Influence of essential amino acids on muscle mass and muscle strength in patients with cerebral stroke during early rehabilitation: protocol and rationale of a randomized clinical trial (AMINO-Stroke Study)
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Influence of essential amino acids on muscle mass and muscle strength in patients with cerebral stroke during early rehabilitation: protocol and rationale of a randomized clinical trial (AMINO-Stroke Study)

机译:早期康复期间必需氨基酸对脑卒中患者肌肉质量和肌肉强度的影响:一项随机临床试验的方案和原理(AMINO-中风研究)

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Patients with stroke are at a high risk for long-term handicap and disability. In the first weeks after stroke muscle wasting is observed frequently. Early post-stroke rehabilitation programs are directed to improve functional independence and physical performance. Supplementation with essential amino acids (EAAs) might prevent muscle wasting and improve rehabilitation outcome by augmenting muscle mass and muscle strength. We aim to examine this in a double blinded, randomized placebo-controlled clinical trial. Patients with ischemic or haemorrhagic stroke will be enrolled at begin of the early post-stroke rehabilitation in a parallel group interventional trial. Oral supplementation of EAAs or placebo will be given for 12?weeks in a double blinded manner. Physical and functional performance will be assessed by exercise testing before supplementation of EAAs as well as at discharge from the in-patient rehabilitation, at 12?weeks and 1?year afterwards. This is the first randomized double-blinded placebo-controlled clinical study aiming to assess the effect of the EAAs supplementation on muscle strength, muscle function and physical performance in stroke patients during early post-stroke rehabilitation. Supplementation of EAAs could prevent muscle mass wasting and improve functional independence after stroke. The study is registered at the German registry for clinical trials as well as at World Health Organization (WHO; number DRKS00005577 ).
机译:中风患者长期残障和残疾的风险很高。在中风后的头几周,经常观察到肌肉消瘦。早期的中风后康复计划旨在改善功能独立性和身体机能。补充必需氨基酸(EAA)可以通过增加肌肉质量和力量来防止肌肉萎缩并改善康复效果。我们旨在通过双盲,随机安慰剂对照临床试验对此进行检查。缺血性或出血性中风的患者将在一项平行组介入试验中,在中风后早期康复开始时入组。以双盲方式口服EAA或安慰剂12周。在补充EAA之前以及在住院康复后的12周和1年后,通过运动测试来评估身体和功能表现。这是首项随机双盲安慰剂对照临床研究,旨在评估EAAs补充剂对卒中后早期康复过程中卒中患者的肌肉力量,肌肉功能和身体机能的影响。补充EAA可以预防中风后肌肉质量的浪费并改善功能独立性。该研究已在德国临床试验注册处以及世界卫生组织(WHO;编号DRKS00005577)中进行了注册。

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