跳至主要内容
临床试验/NL-OMON56139
NL-OMON56139已完成不适用

Validation of the *Vital Signs Monitoring System* classification algorithm for assessment of physical activity in hospitalised patients - Validation of the Vital Signs Monitoring System

Medisch Universitair Ziekenhuis Maastricht0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • - Receiving physiotherapy treatment during hospitalisation at the MUMC+
  • - 18 years or older
  • - Able to walk
  • - Willing to participate
  • - Sufficient understanding of the Dutch language
  • - Able to provide written informed consent.

排除标准

  • A potential subject who meets any of the following criteria will be excluded
  • from participation in this study:
  • - Admitted to the Intensive Care or Medium Care units.
  • - A contraindication concerning walking (as reported by the attending medical
  • specialists in the medical record).
  • - A contraindication to wearing the FastFocus* Vital Signs Monitoring System
  • activity monitor at the ear (i.e.: patients with signs of skin damage on the
  • ear, patients with pierced ears at the sensor application/measurement site,
  • patients with skin conditions that could result in permanent harm when using
  • the EarSensor, patients with limited blood perfusion through the ear due to
  • medical conditions (e.g., cauliflower ears, ischemic ear shells, etc.),
  • patients that are obliged to wear other medical devices for health and/or
  • disability purposes (e.g., hearing aids, oxygen tubes, etc.), and/or patients
  • in which the inner aspect of the ear (cavum conchae) is not large enough to
  • accommodate the hook of the sensor without touching the tragus and/or crus of
  • - Impaired cognition (dementia / delirium) as reported by the attending medical
  • specialist in the medical record.
  • - Incapacitated subjects as reported by the attending medical specialist in the
  • medical record. When any doubt arises, the patient will not be considered
  • - A life expectancy shorter than 3 months as mentioned by the attending medical
  • specialist in the medical record
  • - Subjects that are not allowed to leave their hospital room due to isolation
  • measures as reported in the medical record.
  • - Pregnant or breastfeeding women.
  • - Inability to give informed consent.
  • - Previous participation in this study.

研究者

发起方
Medisch Universitair Ziekenhuis Maastricht

相似试验