At a glance
ClinicalIndex Comparison RecordN/ACompleted· 48 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Reassure Respiration Rate Device: Home User Study
In Brief
An observational study for Ease of Use. Completed, enrolled 48 participants.
Detailed 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.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsEase of Use
Countries--
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartOct 2014
Primary CompletionNov 2015
Study CompletionDec 2015
First PostedApr 2016
TodayJul 2026
First PostedApr 15, 2016
Enrollment StartOct 1, 2014
Primary CompletionNov 1, 2015
Study CompletionDec 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 10.2 years ago