None
Conditions
Interventions
None listed
Sponsors
Kansai Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthcare professionals (midwives, anesthesiologists, and obstetricians) involved in cases of labor analgesia management conducted under the remote support system during weekday off-hours. Individuals who received an explanation of the purpose of this study and the questionnaire survey from the principal investigator, fully understood the explanation, and provided informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: Individuals involved in cases in which remote support was not implemented at any time due to communication failures or other technical problems. Individuals involved in cases in which labor progressed rapidly after the initiation of anesthesia and delivery was completed within a short period without any remote support. Individuals who declined participation in this study. Individuals deemed inappropriate for inclusion as study participants by the principal investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Healthcare professionals involved in the remote clinical support system (midwives, obstetricians, and anesthesiologists) will complete a questionnaire using a five-point Likert scale and free-text responses to evaluate satisfaction with the communication application, perceived usefulness and safety of the remote clinical support system, improvements in interprofessional communication, intention for continued use, and operational challenges. | — |
Countries
Japan
Contacts
Public ContactMICHIKO KANAZAWA
Kansai Medical University Department of Anesthesiology
Outcome results
None listed