Healthy volunteers Not Applicable
Conditions
Interventions
This study has been designed to optimise ambulatory monitoring systems to provide reliable continuous data recording in a clinical setting. This will be done during several rounds of testing and troub
Sponsors
University of Oxford
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Staff working for the Oxford University Hospitals NHS Foundation Trust, in the designated area. 2. Willing and able to give informed consent for the study. 3. Aged 18 or over 4. In good health.
Exclusion criteria
Exclusion criteria: 1. Allergies to adhesives dressings or metals e.g. Nickel. 2. Intra-cardiac device e.g. permanent pacemaker (only applicable to the chest patch monitor).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The proportion of time each vital sign parameter (heart rate, SPO2 and breathing rate) is recorded versus time the device is worn. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. The frequency and duration of data drop-out for each vital sign parameter. 2. The waveform quality of each vital sign parameter. 3. The wear-ability of the device is measured using questionnaires after each time an ambulatory monitor wear session has ended. 4. The availability of data over the 12 hour period, log of issues and crashes. 5. Duration of battery is measured as life from full charge to battery drain. | — |
Countries
United Kingdom
Contacts
Public ContactLouise Young
Outcome results
None listed