跳至主要内容
临床试验/NCT05237518
NCT05237518Unknown不适用

Accuracy Evaluation of EarlySense Device, a Smaller Shape Sensor With BLE Connection to Processing Unit (HUB)) for Use While Two People Are in Bed ("Home Use" Scenario)

EarlySense Ltd.0 个研究点目标入组 36 人开始时间: 2023年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
36
主要终点
Heart Rate (BPM)

研究概览

简要总结

Accuracy evaluation of EarlySense device, a smaller shape sensor with BLE connection to processing unit (HUB)) for use while two people are in bed ("Home Use" scenario) The EarlySense device is intended for continuous contact-free monitoring of heart rate and respiration rate at home, or in professional healthcare settings. The system is intended for remote monitoring of patients by healthcare professionals and is indicated mainly for elderly population monitoring.

The modified version of this product which is the subject of this validation study allows monitoring of subjects when there is a second person in the same bed ("Home scenario" environment). The objective of this study is to evaluate the accuracy of the device in determining Respiration Rate (Br./min) and Heart Rate (BPM) at home environment, while two people are in the same double bed. The study aims to demonstrate that partner presence doesn't affect the monitoring accuracy of the subject that is being measured.

The continuous monitoring will last for duration of 90 minutes for each subject, unless the participant requests termination of the experiment or as per the physician's instructions. Subjects admitted to the study will be monitored using both Capnography and ECG- as reference devices. The EarlySense revised sensor will be placed under one of the two-mattress types incorporated into the study. Both mattresses are typical double bed mattresses of 160 X 200 cm with two different internal structure composition. The sensor will be placed directly below the subject's thorax area on one of the mattress sides. The signals collected by the sensor will be communicated via BLE to the processing unit (HUB).

Following connecting the subject to the reference devices, both the subject and the partner will be instructed on the actions they should perform through the stages of the experiment.

The subject will lie on the mattress side where the EarlySense sensor is located, while the partner will be instructed to enter the other side of the mattress. At this time, the experiment will start, and the clock will start running.

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
是

入选标准

  • •Age above 18 years
  • •Sleeping with a partner in bed
  • •Willing to sign the consent form

排除标准

  • •Subjects with arrhythmia will be excluded from the study

研究组 & 干预措施

36 adults

Other

The test group should include both men and women subjects. Two equal sizes (18) sub-groups will be enrolled such that each sub-group will be monitored while lying on a different mattress type.

干预措施: EarlySense Noomi system (Device)

结局指标

主要结局

Heart Rate (BPM)

时间窗: 90 minutes

Measurement obtained from study device will be compared to measurement obtained from SOC device.

Respiration Rate (Br./min)

时间窗: 90 minutes

Measurement obtained from study device will be compared to measurement obtained from SOC device.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

相似试验