Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Continuous Vitals Monitoring - Department of Anesthesia at PHC
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Collect patient and clinicians' feedback about the CCPC Platform
研究概览
简要总结
To confirm feasibility and accessibility of the CCPC Platform (Oxymotion, Bridge Health Solutions medication adherence software, CloudDX home kit) in two different environments - in hospital and at-home, in patients undergoing non-cardiac surgery.
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
- 19 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •19 years or older
- •Patients that have undergone a non-cardiac surgery at SPH requiring an inpatient hospital stay
- •Peri-op patients who are in the Surgical High Acuity Unit (SHAU) and those followed by Anesthesia Perioperative Outreach team on the ward
- •Living within British Columbia, Canada and in an area that is covered by Bell cellular network
排除标准
- •Patient refusal
- •Lack of capacity to consent to the study (including having received sedative or general anesthetic within the past 24 hours)
- •Unable to use (or does not have a caregiver who can help put on) study monitoring device at home
- •Unable to complete (or does not have a caregiver who can help complete) study questionnaires by electronic (mobile, tablet, or computer), paper, nor phone
- •No access to cell phone nor landline at home to receive follow-ups
- •Preoperatively known to be discharged to a nursing home or rehabilitation facility
- •Known allergic reactions to any part material of study devices
结局指标
主要结局
Collect patient and clinicians' feedback about the CCPC Platform
时间窗: From enrollment to the end of follow up at 10 days
This will be completed via an assessment of the quantitative data on how long and how often patients use this monitoring and what were the reasons that patients took the monitors on and off.
Confirm the technical goals of the CCPC platform are met.
时间窗: From enrollment to the end of follow up at 10 days
This will be completed by ensuring clinical workflow is met when using the monitoring platform.
次要结局
未报告次要终点