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Usability Evaluation - Reassure Respiration Rate Device: Home User Study

NCT02740517 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 48

Last updated 2021-05-07

Study results available
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Summary

This is a usability evaluation of the Reassure device. The device is a non-contact device which passively monitors breathing.

The purpose of this usability evaluation is to understand any issues that the intended user population have while using the device unsupervised in the home and to determine if the device can collect data that is of sufficient quality to be successfully analysed for respiration rate.

Conditions

  • Ease of Use

Sponsors & Collaborators

  • ResMed

    lead INDUSTRY

Principal Investigators

  • Paul Phillips, MA, MSc · ResMed Sensor Technologies Ltd

Eligibility

Min Age
30 Years
Max Age
95 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-10-31
Primary Completion
2015-11-30
Completion
2015-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02740517 on ClinicalTrials.gov