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临床试验/NCT02740517
NCT02740517已完成不适用

Reassure Respiration Rate Device: Home User Study

ResMed0 个研究点目标入组 48 人开始时间: 2014年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
ResMed
入组人数
48
主要终点
Percentage of Nights' Data That Were Successfully Recorded

研究概览

简要总结

This is a usability evaluation of the Reassure device. The device is a non-contact device which passively monitors breathing.

The purpose of this usability evaluation is to understand any issues that the intended user population have while using the device unsupervised in the home and to determine if the device can collect data that is of sufficient quality to be successfully analysed for respiration rate.

详细描述

The aim of the set of Reassure Home User Trials is to understand any usability issues that users have while using the Reassure non contact monitor in their home environment.

Other objectives:

  • To gather useful feedback on the user interface and suggestions for its improvement.
  • To gather information on the device stability in the more variable conditions of the home user environment.
  • To gather data in order to demonstrate compliance with IEC62366, and thus IEC60601-1

The users had the device for a minimum of 10 nights, to confirm if the device could be used for an extended period and the likely compliance rates of users

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

年龄范围
30 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • volunteer, no previous exposure to the device

排除标准

  • restless leg syndrome or other conditions giving to uncontrolled movements whilst asleep

结局指标

主要结局

Percentage of Nights' Data That Were Successfully Recorded

时间窗: At least 10 nights

The definitions utilised to determine the patient's success or otherwise at making a recording of their sleep respiration data are: • That 67% of the duration of the recording has to be of sufficient quality for the respiration rate algorithms to be able to discern a respiration rate. AND • The duration of analysable data is to be at least 2 hours.

次要结局

  • Percentage of Recordings With Successful First Time Transmission(For at least 10 nights of recordings)

研究者

发起方
ResMed
申办方类型
Industry
责任方
Sponsor

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