Respiratory Monitoring in Neonates
Conditions
Interventions
Conventional Respiratory Monitoring Group:Respiratory monitoring performed with conventional monitoring technology
Radar-Based Non-Contact Monitoring Group:Radar-Based Non-Contact Monitoring
Wireless Vital-signs Pod (Vpod) Group:Wireless Vital-signs Pod
Sponsors
Beijing Childrens Hospital,Capital Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Research Content One: Preterm infants with a gestational age of 24 to 44 weeks; 2. Research Content Two: (1) Family respondents: Primary caregivers of hospitalized children aged 0 to 2 years, who have participated in FICare care at least once; (2) Healthcare provider respondents: Working in the NICU or related pediatric surgical wards, directly involved in using VPod or providing care for children using VPod, including clinical nurses, doctors (neonatology or pediatric surgery), and biomedical engineers. 3. Research Content Three: (1) Preterm infants with a gestational age of >=28 weeks; (2) Preterm infants requiring NCPAP treatment due to respiratory distress, or those needing NCPAP support after weaning from invasive mechanical ventilation.
Exclusion criteria
Exclusion criteria: 1. Research Content One: (1) Vital signs are extremely unstable and require frequent emergency treatment; (2) Hospital stay is less than 24 hours; (3) Clinicians deem the patient unsuitable to participate in this clinical trial. 2. Research Content Two: (1) Family respondents: The child under their care is extremely unstable during the study period, making safe handling or movement impossible; the respondent is unable to provide informed consent themselves; (2) Healthcare staff respondents: Those who do not directly interact with or manage the relevant child or equipment. 3. Research Content Three: (1) Has major congenital malformations (such as complex congenital heart disease, severe chromosomal abnormalities, etc.); (2) In terminal condition or expected survival <24 hours.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Respiratory Monitoring Sensitivity;Performance of the Wireless Vital-signs Pod;Rate of Effective Alarms for Abnormal Critical Physiological Parameters;Composite Adverse Event Rate; | — |
Countries
China
Contacts
Public ContactHei Mingyan
Beijing Childrens Hospital,Capital Medical University
Outcome results
None listed