Skip to main content
Clinical Trials/NL-OMON48983
NL-OMON48983
Completed
N/A

Feasability Assessment of wearable sensors for continuous ambulatory vital signs monitoring - Vital signs monitoring with wearable sensors

Divisie Vitale Functies0 sites10 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Divisie Vitale Functies
Enrollment
10
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Divisie Vitale Functies

Eligibility Criteria

Inclusion Criteria

  • 10 volunteers of both sexes (\*18 years of age) are eligible for enrolment, with
  • the following criteria:
  • \* 5 volunteers need to be at age 65 or above
  • \* 3 volunteers need to have a BMI \>30 kg/m2, Study 2
  • 10 volunteers ( \*18 years of age) are eligible for enrolment, with the
  • following criteria:
  • \* At least one hospitalization requiring monitoring in the past two years
  • (\*former patients\*)
  • \* Currently healthy or in a stable phase of chronic illness
  • \* 3 volunteers need to have a BMI \>30 kg/m2

Exclusion Criteria

  • \* Known allergy/skin irritation to the adhesives used in the sensor patches.
  • \* Implanted active medical devices, such as a cardioverter defibrillator or a
  • \* Current pregnancy
  • \* Inability to give informed consent

Outcomes

Primary Outcomes

Not specified

Similar Trials