ACTRN12624000447550招募中Unknown
sing wearable activity trackers to promote activity during rehabilitation in inpatients and outpatients at a rehabilitation hospital: a single-group feasibility study.
niversity of South Australia0 个研究点目标入组 30 人开始时间: 2024年4月11日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 发起方
- 入组人数
- 30
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
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •Virtual Rehabilitation Ward
- •18 years old, able to ambulate independently or with stand-by assistance/supervision, have a rehabilitation goal related to increasing mobility/activity, expected length of stay of at least 2 weeks.
- •FIT Program
- •18 years old, able to ambulate independently or with stand-by assistance/supervision, own an Apple or Android smartphone (to download Fitbit application to use with Fitbit WAT device) have a rehabilitation goal related to increasing mobility/activity.
排除标准
- •Virtual Rehabilitation Ward
- •Lower limb amputation, delirium or cognitive impairment impacting ability to follow instructions or engage with independent behaviour change, not expected to ambulate during admission, insufficient English language to comprehend instructions regarding WAT use or no available interpreter, inadequate vision or dexterity to use devices and no available carer to help, any absolute contraindication to partaking in exercise (e.g. symptomatic severe aortic stenosis, unstable angina).
- •FIT Program
- •Lower limb amputation, delirium or cognitive impairment impacting ability to follow instructions or engage with independent behaviour change, not expected to ambulate during admission, insufficient English language to comprehend instructions regarding WAT use or no available interpreter, inadequate vision or dexterity to use devices and no available carer to help, any absolute contraindication to partaking in exercise (e.g. symptomatic severe aortic stenosis, unstable angina).
研究者
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