Pijnmanagement bij neonaten Neonatal discomfort Pain in newborns
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Primary outcome (Effectiveness evaluation): - Patients admitted to the NICU of the Erasmus MC-Sophia Children*s Hospital during the pre- and post-implementation phases of the study. Secondary outcomes (Implementation process evaluation): - Healthcare professional (e.g., physician, nurse, nurse-specialist) or parents of patients that has been exposed to TMD.
Exclusion criteria
Exclusion criteria: Primary outcome (Effectiveness evaluation): - Patients not admitted and discharged during the pre- or post-implementation phase. Secondary outcomes (Implementation process evaluation): - n/a
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| The evaluation of the implementation process will assess implementation outcomes, including acceptance, appropriateness, adherence to the protocol, and penetration. | — |
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is to assess the effectiveness of Telemedrics in improving patient comfort in the NICU, measured by the reduction in the duration of inadequately treated discomfort in neonates. | — |
Countries
Netherlands