Skip to content

Mobile Chat Service for Parents of Children in Pediatric Emergency Room

Mobile Chat Service for Parents of Children in Pediatric Emergency Room: A Randomized Control Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06002542
Enrollment
60
Registered
2023-08-21
Start date
2023-07-20
Completion date
2023-10-31
Last updated
2023-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emergency Medicine, Medical Informatics, Pediatric Emergency Medicine

Brief summary

The goal of this clinical trial is to test giving all medical/non-medical information in the pediatric emergency room(ER). Main questions it aims to answer are: * Does providing medical/non-medical information to parents of patients visiting the emergency room raise the satisfaction with the ER visit? * Does providing medical/non-medical information to parents of patients visiting the emergency room lower the workload of medical staff? 60 participants will be randomly assigned to treatment group and control group. Both groups will communicate freely with the researchers through mobile chat service. Treatment group will get information of medical/non-medical information in emergency room and control group will get information if they need. Before leaving the emergency room, both group will fill out a questionnaire related to satisfaction with the emergency room visits. 5 out of 30 participants of each group will be interviewed about their satisfaction with service. 10 nurses in charge of patients participating in the study record the number of questions directly received and 5 out of 10 nurse will be interviewed about their nursing experience for participants using mobile chatbot service. Researchers will compare treatment group and control group to see if providing medical/non-medical information raise the satisfaction with emergency room visits.

Detailed description

The goal of this clinical trial is to test giving all medical/non-medical information in the pediatric emergency room. Main questions it aims to answer are: * Does providing medical/non-medical information to parents of patients visiting the emergency room raise the satisfaction with the ER visit? * Does providing medical/non-medical information to parents of patients visiting the emergency room lower the workload of medical staff? Design : 60 participants will be randomly assigned to treatment group and control group. Both groups will communicate freely with the researchers through mobile chat service. Treatment group will get information of medical/non-medical information in emergency room and control group will get information if they need. Before leaving the emergency room, both group will fill out a questionnaire related to satisfaction with the emergency room visits. 5 out of 30 participants of each group will be interviewed about their satisfaction with service. 10 nurses in charge of patients participating in the study record the number of questions directly received and 5 out of 10 nurse will be interviewed about their nursing experience for participants using mobile chatbot service. Researchers will compare treatment group and control group to see if providing medical/non-medical information raise the satisfaction with emergency room visits.

Interventions

BEHAVIORALInformation provided

get information at every stage of care in emergency room

BEHAVIORALControl

Information is only provided when participants request it.

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

open-label randomized control trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age ≥ 18 years * Parents of patients whose KTAS(Korean Triage and Acuity Scale) is 2, 3, 4. * Parents of patients whose chief complaints are fever, abdominal pain, dyspnea, nausea and vomiting, and skin rash. * Those who voluntarily agreed to participate in the study.

Exclusion criteria

* Those who didn't consent to participate in the study. * Parents of patients whose KTAS(Korean Triage and Acuity Scale) is 1 or 5. * Those who doesn't use mobile phone or those who don't have the appropriate level of consciousness to send and receive messages.

Design outcomes

Primary

MeasureTime frameDescription
ED CAHPS(Emergency department Consumer Assessment of Healthcare Providers and System) Questionnaire score at dischargeDischarge time, 6 hours on average from arriving emergency room.ED CAHPS is a survey instrument for measuring patients' experience of care in emergency department.

Secondary

MeasureTime frameDescription
Interview for participantsAfter leaving the emergency room visit, within 48hoursInterview on the experience and satisfaction of using mobile chatbot services

Other

MeasureTime frameDescription
Questions to nurseaverage of 6 hours from the time participants arrived at the emergency room to discharge.The nurse in charge counts the number of questions received from participants.
Interview for nurseAfter work, within 48hours after nursing participants.Interviewing whether chatbot services lower their tasks

Countries

South Korea

Contacts

Primary ContactMinha Kim, MD
mhh.kim@samsung.com82-2-3410-2061

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026