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The aim of this clinical pilot study is to evaluate the validity, acceptability and usability of the newborn bed monitoring device among newborns, parents and healthcare professionals in hospital environment. The specific aims for the study are to:
The participating newborns will be sleeping on the bed monitoring device for two hours and the measurements of the device will be compared with the reference device (golden standard). The acceptability and usability will be assessed by parents and healthcare professionals by fulfilling a questionnaire and participating in interviews.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Newborn | Newborn is sleeping in the bed monitoring device for two hours | ||
| Parents | Parents of the newborns participating in the study. | ||
| Healthcare professionals | Healthcare professionals participating in newborn care. |
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| Measure | Description | Time Frame |
|---|---|---|
| Heart rate | Two hours from the beginning of the data collection |
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Inclusion Criteria for newborns:
Inclusion criteria for parents:
Inclusion criteria for healthcare professionals:
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All parents will be informed about the study when moving from labour ward to postnatal ward. Newborns participating in the study will be approximately 1-3 days old. Parents of the participating newborns will be informed about the study and invited to participate to the study part for parents.
All healthcare professionals working in the study unit during the newborn data collection are able to participate in the study part for healthcare professionals.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Turku University Hospital | Turku | Finland |
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