跳至主要内容
临床试验/NCT04480411
NCT04480411撤回不适用

Use of Technology and Telemedicine to Improve Quality of Care in COVID 19 Patients

Stanford University1 个研究点 分布在 1 个国家开始时间: 2022年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Patient provider experience survey score

研究概览

简要总结

The purpose of this study is to assess the use of technology including remote vital sign monitoring in improving quality of patient care, decreasing hospital admissions and re-admissions, decreasing hospital length of stay and decreasing use of personal protective equipment.

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
否

入选标准

  • •Hospitalized patient with COVID 19 or outpatient under investigation for or diagnosed with COVID 19
  • •Clinically stable (on 4L O2 or less, non ICU)
  • •Demonstrates ability to be trained in use of digital stethoscope technology

排除标准

  • •Pregnancy

研究组 & 干预措施

COVID-19 Patients

Experimental

Patients that are admitted to the hospital with COVID 19.

干预措施: Doctorgram Patient Kit (Behavioral)

结局指标

主要结局

Patient provider experience survey score

时间窗: Once after completion of device use (up to 15 minutes to complete the survey)

Five questions related to satisfaction with experience using home pulse oximetry, each on a scale of 1 (poor) to 5 (excellent) summed and averaged for an overall range of 1 to 5 (higher scores = better experience).

Provider experience survey score

时间窗: Once after completion of device use (up to 15 minutes to complete the survey)

Four questions related to satisfaction with experience using home pulse oximetry, each on a scale of 1 (poor) to 5 (excellent) summed and averaged for an overall range of 1 to 4 (higher scores = better experience).

Use of personal protective improvement

时间窗: 6 months

Level of personal protective improvement in an in-patient setting.

Number of in-patient encounters with COVID patients as a measure of provider exposure to high risk illness

时间窗: 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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