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Clinical Trials/NL-OMON56139
NL-OMON56139
Completed
Not Applicable

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 sites50 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patiënten met problemen met bewegend functioneren
Sponsor
Medisch Universitair Ziekenhuis Maastricht
Enrollment
50
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
November 8, 2023
Last Updated
last year
Study Type
Observational non invasive

Investigators

Sponsor
Medisch Universitair Ziekenhuis Maastricht

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Not specified

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