Mobile Chat Service for Parents of Children in Pediatric Emergency Room

Sponsor
Samsung Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT06002542
Collaborator
(none)
60
1
2
3.4
17.7

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Information provided
  • Behavioral: Control
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
open-label randomized control trialopen-label randomized control trial
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Mobile Chat Service for Parents of Children in Pediatric Emergency Room: A Randomized Control Study
Actual Study Start Date :
Jul 20, 2023
Anticipated Primary Completion Date :
Oct 31, 2023
Anticipated Study Completion Date :
Oct 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Information provided

Participants are invited to the chat room and receive messages, which include the stages of their medical care, information about tests and medications, and non-medical information such as directions to pharmacy and parking information.

Behavioral: Information provided
get information at every stage of care in emergency room

Experimental: Control

Participants are invited to the chat room and they can get information when they request it.

Behavioral: Control
Information is only provided when participants request it.

Outcome Measures

Primary Outcome Measures

  1. ED CAHPS(Emergency department Consumer Assessment of Healthcare Providers and System) Questionnaire score at discharge [Discharge 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 Outcome Measures

  1. Interview for participants [After leaving the emergency room visit, within 48hours]

    Interview on the experience and satisfaction of using mobile chatbot services

Other Outcome Measures

  1. Questions to nurse [average 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.

  2. Interview for nurse [After work, within 48hours after nursing participants.]

    Interviewing whether chatbot services lower their tasks

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Samsung Medical Center Seoul Gangnam Korea, Republic of 06351

Sponsors and Collaborators

  • Samsung Medical Center

Investigators

  • Study Director: Wonchul Cha, PhD, Samsung Medical Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Samsung Medical Center
ClinicalTrials.gov Identifier:
NCT06002542
Other Study ID Numbers:
  • TMI
First Posted:
Aug 21, 2023
Last Update Posted:
Aug 21, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 21, 2023