NCT07537478已完成不适用
Respiration Measured Via End-tidal CO2 and Spirometry Study
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 2
- 主要终点
- Respiratory rate detection - end tidal CO2
研究概览
简要总结
To collect respiration data via end-tidal CO2 and spirometry and compare respiration rates measured via the two methods.
详细描述
This is a non-randomized, data collection study that will enroll up to 50 participants.
There will be one study visit per participant and no follow up period.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
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
- •Willing and able to provide informed consent
- •Age 18 or above
- •Full time or part time BSC employee
- •Willing and able to participate in the required testing
排除标准
- •Currently enrolled in another clinical trial that might interfere with data collection or placement of the study system
- •Subject is pregnant as indicated by subject report
- •Known allergy or sensitivity to materials used in the study (Neoprene, Nylon)
- •Any past or current medical event that could represent a risk for the subject to perform the study required activities in the opinion of the investigator
研究组 & 干预措施
Wearable respiration mask - Exercise
Healthy control subjects eligible for exercise.
干预措施: Wearable Respiration mask - exercise (Device)
Wearable respiration mask
Healthy control subjects not eligible for exercise.
干预措施: Wearable respiration Mask (Device)
结局指标
主要结局
Respiratory rate detection - end tidal CO2
时间窗: From enrollment through the end of the data collection visit, expected to take up to 3 hours.
End-Tidal CO2 will be measured as a fractional concentration (volume percent of CO₂ in exhaled gas).
次要结局
- Respiratory rate detection - spirometry(From enrollment through the data collection visit, up to 3 hours.)
研究者
研究点 (2)
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