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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04719520
Other study ID # 202010016RINA
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 23, 2021
Est. completion date February 28, 2022

Study information

Verified date February 2022
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

As the number of operation increases, it is important to control of the utilization rate of the operating room. This study is a comparative study of the benefits of different ways of contacting patients' family members during surgery.


Description:

As the number of operation increases, it is important to control of the utilization rate of the operating room. When family members need to be contacted during the operation, whether family members in the waiting area can be notified in time will affect the overall operation time of the patient and the utilization rate of the operating room. The way of contact also indirectly affects issues such as hospital costs and patient privacy. This study is a comparative study of the benefits of different ways of contacting patients' family members during surgery. This study will compare the current traditional method (using radio and telephone to notify the patient's family to the operating room) or the wireless vibrating caller to notify the patient's family to the operating room, and analyze the variables generated by the two different methods including demand time of notification, acceptance, and patient privacy issues. The results of the study will use scientific data to prove which way to notify the patient's family is more efficient and a good way to take into account of the patient's privacy.


Recruitment information / eligibility

Status Completed
Enrollment 68
Est. completion date February 28, 2022
Est. primary completion date September 30, 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion criteria: - The care family of surgical patients Exclusion criteria: .The surgical patient's care family has the problems of impaired hearing activity or walking disability.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
wireless vibrating caller
using the wireless vibrating caller to notify the patient's family to the operating room

Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary demand time demand time of notifying the patient's family 1 day
Secondary acceptance Questionnaire to assess the acceptance the notifying system by the patient's family 1 day
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