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临床试验/NCT06395350
NCT06395350已完成不适用

Spire Health Remote Patient Monitor Human Factors Summative Study Protocol

Spire, Inc.2 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2019年9月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Spire, Inc.
入组人数
17
试验地点
2
主要终点
Assess the participant's ability to perform essential tasks related to handling of device measured by Pass/Fail

研究概览

简要总结

This usability validation testing protocol outlines the methods being used to demonstrate and gather evidence that the current design and user experience of the Spire Remote Patient Monitor are safe and effective for use by the people who are representative of the intended users under expected use conditions. This summative testing is the culmination of several preliminary analyses including a formative usability evaluation via Cognitive Expert Review Panel and is intended to assess the effectiveness of control measures put in place to reduce/eliminate use-related hazards or potential use errors.

详细描述

The summative testing will address user interactions with all components of the Spire Remote Patient Monitor related to tasks associated with the user group, including the Medical Health Tags, SpireHealth Mobile Application and Healthcare Provider Dashboard. This protocol specifies the required testing methods and associated acceptance criteria, as well as other information necessary to collect that evidence.

This human factors summative test is aimed to uncover the following:

  • Determine if the final system design is safe and effective for use by the intended users in the intended use environment
  • Investigation of any use errors related to risk observed
  • To identify any potential new use errors relating to risk Background

Empirical activities in the form of a Cognitive Expert Review Panel was conducted to evaluate design iterations on critical tasks prior to summative testing. The results of these activities were used to improve UI design and inform analytical analyses such as task analysis, PCA analysis and use error analysis (DOC-75057 Use Error Analysis) This validation includes all Spire Remote Patient Monitor system interfaces associated with the primary consumer user groups.

The Spire Remote Patient Monitor that are the subject of this validation need to be supported by the following devices:

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

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

入选标准

  • Must indicate that they are interested in using a smartphone and/or wearable fitness device for tracking their health
  • High school degree or equivalent (e.g., GED) or less - at least 2
  • Some college but no degree or associate degree - at least 4
  • Age 22-49 - at least 5
  • Age 50-65 - at least 5
  • Age Over 65 - at least 2
  • Near even split of men and women
  • Almost never limited by my physical condition
  • Rarely limited by my physical condition
  • Occasionally limited by my physical condition
  • Often limited by my physical condition
  • Almost always limited by my physical condition
  • Users with iPhone experience
  • Smart Phone Savviness
  • No more than 7 users who own use a wearable fitness device
  • Wearable Fitness Device savviness

排除标准

  • Participant currently works in tech industry
  • Participant or a member of his/her household currently works for any company that develops, manufactures, or sells smartphones or smart wearable fitness devices
  • Participant has participated in market or user research related to a medical device within the last 6 months and has participated in more than 2 in the last 3 years
  • Participants are trained clinicians or healthcare providers

结局指标

主要结局

Assess the participant's ability to perform essential tasks related to handling of device measured by Pass/Fail

时间窗: 60 minutes

Observational techniques will be used to assess the participant's ability to easily use various features on the device and discover whether user errors occur.

次要结局

未报告次要终点

研究者

发起方
Spire, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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