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CommunicationNCT04719520

Efficiency Analysis of Wireless Vibrating Caller During Surgery

A study testing wireless vibrating caller in people with Communication, run by National Taiwan University Hospital at 1 site in Taiwan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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. Read more about this study

Who is it for?
Ages 20 to 80 years
Conditions the study is for
Communication
What is being tested?
wireless vibrating caller
Could I receive a placebo?
No, everyone receives an active treatment
How many people
68 participants
Where
1 siteTaiwan
Study dates
23 Feb 2021to 28 Feb 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • The care family of surgical patients

Who cannot join

  • .The surgical patient's care family has the problems of impaired hearing activity or walking disability.

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • National Taiwan University Hospital

    Taipei, 10002

Other trials in Taiwan

About this study

Official title: Efficiency Analysis of Wireless Vibrating Caller Compared With Traditional Broadcasting in Contacting Patients' Family Members During Surgery

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.

Read the detailed 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.

Conditions
Communication
Being tested
wireless vibrating caller
Keywords
Operating room; Telecommunication experts
Medical subject headings
Communication

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • wireless vibrating callerBehavioural

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

Study groups in NCT04719520
Study groupRoleWhat they receive
traditional methodNo interventionradio and telephone to notify the patient's family to the operating room
wireless vibrating callerExperimentalusing the wireless vibrating caller to notify the patient's family to the operating room
Receives: Behavioral: wireless vibrating caller

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. demand time

    demand time of notifying the patient's family

    Measured: 1 day

Secondary outcomes (1)
  1. acceptance

    Questionnaire to assess the acceptance the notifying system by the patient's family

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jan 2021
  2. Study start23 Feb 2021
  3. Primary completion30 Sep 2021
  4. Study completion28 Feb 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Model description
This study is a comparative study of the benefits of different ways of contacting patients' family members during surgery.
Masking
None (open label)
Enrolment
68 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04719520
Sponsor's protocol ID
202010016RINA
Status last verified
Feb 2022
First submitted
17 Jan 2021
Last updated
2 Mar 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing wireless vibrating caller in people with Communication, run by National Taiwan University Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Mar 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

demand time (time frame: 1 day). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Mar 2022.

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