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

NCT ID: NCT06739746

Last Updated: 2025-05-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

400 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-06-01

Study Completion Date

2025-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Noise Exposure

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Medical staff group

Investigate the demographic information and subjective perception of noise among medical staff in the post anesthesia care unit.

No intervention measures

Intervention Type OTHER

No intervention measures

Hospital Group

Investigate the staffing, size, number of beds, noise levels, etc. of post anesthesia care unit in different hospitals.

No intervention measures

Intervention Type OTHER

No intervention measures

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

No intervention measures

No intervention measures

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Shenzhen Mindray Bio-Medical Electronics Co., Ltd

UNKNOWN

Sponsor Role collaborator

First Affiliated Hospital of Chongqing Medical University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Min Su

Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Su Min Min

Role: CONTACT

8613568235251

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2024-214-01

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.