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Clinical Trials/NCT02805192
NCT02805192CompletedNot Applicable

Validation of a Smart Phone App to Non-invasively Measure the Size of Children

University of Zurich2 sites in 1 country627 target enrollmentStarted: January 30, 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
627
Locations
2
Primary Endpoint
Comparison of the size measured by the smart phone app with the child's size.

Study Overview

Brief Summary

Smart phones are omnipresent. Apps exist to calculate size of medical equipment and doses of medication if a valid weight or age is entered. During emergency situations, these values are often unknown. An App has been developed to measure the size of a child noninvasively. This App is now to be validated in clinical practice. App measured size is calculated and compared to the real size of a child. Via known percentiles of age/weight of the child is calculated upon the App measured size. This value is compared to the mother's, physician's and nurses estimation of the size and weight.

Depending on the size multiple algorithms exist to estimate weight, age and medical values. ("Kindersicher ®", "Notfalllineal ®" and "Broselow Tape ®"). These estimations by the calculations will also be compared to actual weight and age.

Children from 0-12 years of age are included in the emergency Department of the Children's Hospital of the University of Zurich after informed consent obtained by the parents. No therapy decisions from these calculations will be made. The therapy is independent of this study.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
— to 12 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • male and female patients 0-12 years of age (45 per age group)
  • obtained informed consent
  • admitted to the emergency department of the Children's Hospital of the University of Zurich

Exclusion Criteria

  • physically or mentally unable for measurement
  • denial of informed consent

Outcomes

Primary Outcomes

Comparison of the size measured by the smart phone app with the child's size.

Time Frame: immediate, no follow up

Secondary Outcomes

  • Comparison of the estimations calculated upon the smart phone measured size (via known percentiles) with the real age and weight.(immediate, no follow up)
  • Comparison of estimations by parents, physicians and nurses with the actual size and weight.(immediate, no follow up)
  • Comparison of estimations by "Kindersicher ®", "Notfalllineal ®" and "Broselow Tape ®" with real age and weight.(immediate, no follow up)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Philipp Stein

Dr. med. Philipp Stein

University of Zurich

Study Sites (2)

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