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Not yet recruiting NCT06739746

Research on the Sources of Noise in Post Anesthesia Care Unit and the Impact of Noise on Medical Staff

— Observational Noise Exposure

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No intervention measures.
Who it may be relevant to
Registry conditions: Noise Exposure. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The study aims to clarify the sources and influencing factors of noise in the post anesthesia care unit, as well as the perception of noise by medical staff through survey table, in order to improve the noise environment, optimize noise management, protect medical staff, and enhance medical quality.

Interventions

  • Other No intervention measures
    No intervention measures

Primary outcome measures

  • Main noise decibel [Time frame: From enrollment to the end of observation at 1 week]
Secondary outcome measures (12)
  • Secondary noise decibel [Time frame: From enrollment to the end of observation at 1 week]
  • Area of post anesthesia care unit [Time frame: From enrollment to the end of observation at 1 week]
  • Number of beds of post anesthesia care unit [Time frame: From enrollment to the end of observation at 1 week]
  • Medical personnel allocation situation [Time frame: From enrollment to the end of observation at 1 week]
  • Staying time in post anesthesia care unit of patients [Time frame: From enrollment to the end of observation at 1 week]
  • Number of patients with or without tracheal intubation retained [Time frame: From enrollment to the end of observation at 1 week]
  • Daily working hours of medical staff [Time frame: From enrollment to the end of observation at 1 week]
  • Working years of medical staff [Time frame: From enrollment to the end of observation at 1 week]
  • Subjective perception of noise by medical personnel [Time frame: From enrollment to the end of observation at 1 week]
  • The impact of noise on the work of medical personnel [Time frame: From enrollment to the end of observation at 1 week]
  • The source of noise as perceived by the medical staff [Time frame: From enrollment to the end of observation at 1 week]
  • Satisfaction of medical staff with the current noise situation [Time frame: From enrollment to the end of observation at 1 week]

Eligibility criteria

Inclusion criteria

  • Currently working as nurses, doctors, or technicians in the Post Anesthesia Care Unit;
  • Have at least continuous 6 months of work experience in the Post Anesthesia Care Unit;
  • Able to read and answer questionnaires in Chinese fluently.

Exclusion criteria

  • Have hearing impairments or other conditions affecting auditory perception;
  • Have participated in similar studies and completed related surveys within the past 6 months.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06739746 · 2024-214-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗