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Medical InformaticsNCT05847803

Patient Monitoring in the Intensive Care Unit

An observational study of Medical Informatics and Intensive Care, run by Second Affiliated Hospital, Zhejiang University, School of Medicine at 1 site in China.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

a cross-sectional survey of nurses' perception of patient monitoring in the ICUs Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Medical Informatics, Intensive Care
How many people
240 participants
Where
1 siteChina
Study dates
5 Feb 2023to 15 May 2023
Phase
Observational
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: registered nurses in the ICUs

Who may be able to join

  • registered nurses in the ICUs

Who cannot join

  • -

Trial locations and contacts

1 site in 1 country.

Wen Gao, PhD contact

wgao@zju.edu.cn

China1 site, 1 recruiting
  • SAHZhejiangU

    Hangzhou, 310009

    Jingfen Jin, MD, 86-13757118239, zrjzkhl@zju.edu.cn

    Recruiting

Other trials in China

About this study

Official title: Nurses' Perceptions of Patient Monitoring in the Intensive Care Unit: a Cross-sectional Study

a cross-sectional survey of nurses' perception of patient monitoring in the ICUs

Being tested
No intervention, questionnaire survey

What participants receive

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

  • No intervention, questionnaire surveyOther

    No intervention, questionnaire survey

What is being measured

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

  1. clinical requirements of patient monitoring in ICUs

    Assessed using a web-based 36-item survey questionnaire Patient Monitoring in the Intensive Care Unit

    Measured: 12 months of working

  2. Work-related flow in ICUs

    Assessed using the Work-related Flow inventory (WOLF)

    Measured: 12 months of working

Timeline

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

  1. First posted8 May 2023
  2. Study start5 Feb 2023
  3. Primary completion30 Apr 2023 (estimated)
  4. Study completion15 May 2023 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Case crossover
Time perspective
Cross-sectional
Enrolment
240 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05847803
Sponsor's protocol ID
20230110
Status last verified
Jan 2023
First submitted
5 Apr 2023
Last updated
8 May 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Medical Informatics and Intensive Care, run by Second Affiliated Hospital, Zhejiang University, School of Medicine at 1 site in China.

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: status not confirmed, as of the sponsor's last update on 8 May 2023. 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 China. 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?

Results are not available in the source record.

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

Contact Wen Gao (18989879710, wgao@zju.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

clinical requirements of patient monitoring in ICUs (time frame: 12 months of working). The study lists 2 primary outcomes in all. 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 8 May 2023.

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