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临床试验/ACTRN12610000460000
ACTRN12610000460000尚未招募未知

'Strength for Task Training’ to optimise locomotor function following stroke: A pilot randomised controlled trial.

AUT University0 个研究点目标入组 20 人开始时间: 2010年6月4日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • All people aged over 18 years with a single disabling supratentorial ischaemic stroke or intracerebral haemorrhage (Rankin 2-3); between 3-9 months post stroke at the start of the intervention; with a gait speed of between 0.05m/s -<1.2m/s at entry to the study; who are able to walk with or without aid and with or without standby assistance will be eligible for recruitment.

排除标准

  • Individuals will be excluded if: (a) their behaviour would interfere with participation in a group setting, as noted during initial assessment (e.g., agitation, aggression); (b) they have a significant cognitive deficit ((Mini-Mental State Examination (MMSE) Score <23); (c)they are unable to follow a 1 step English verbal command; (d) they are unable to give informed consent; (e) they are medically unstable in the opinion of a medical clinician; (f) they are participating in another study that, in the opinion of the investigator, may affect gait speed or add significantly to participant’s burden; (g) they have excessive pain in any joint that could limit participation; or (h) they have another condition that could impact results (e.g., substance abuse, significant mental illnesses such as major depression) (i) they have any contra-indications to TMS, including pacemaker, artificial heart valves, other metal implants, pregnancy, skull abnormalities, history of seizures or epilepsy, taking medications that may lower seizure threshold, or claustrophobia.

研究者

发起方
AUT University

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