ISRCTN71683182已完成不适用
se of a rehabilitation monitoring device to improve quality of life in patients with recent stroke: a randomised controlled trial
nidad de Conocimiento y Evidencia, Universidad Peruana Cayetano Heredia0 个研究点目标入组 20 人开始时间: 2017年7月3日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 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
入排标准
- 性别
- All
入选标准
- •1. Have suffered an ischemic stroke at least 6 months ago/in the last 6 months, according to their clinical record
- •2. Be over 18 years of age
- •3. Dependency level from A to D according to the Katz Index
- •4. Have verbal permission from their rehabilitation physician to use the device
- •5. Have access to an Android phone during their rehabilitation
- •6. Have a caregiver or a person responsible for attending their basic care
- •7. Give written informed consent to participate in the study
- •Caregivers:
- •1. Be responsible for assisting the post-stroke patient
- •2. Be over 18 years of age
- •3. Give written informed consent to participate in the study
- •4. Be able to use mobile phone applications and understand instructions
- •5. Do not have/suffer from moderate or severe cognitive, visual or auditory impairment
排除标准
- •Does not meet inclusion criteria
研究者
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