Noise Impact in the Post-anesthesia Care Unit

NCT ID: NCT03537820

Last Updated: 2018-10-29

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

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Recruitment Status

COMPLETED

Total Enrollment

816 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-03-05

Study Completion Date

2018-05-04

Brief Summary

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World health organization recommends noise level should be less than 30db in hospital. However many analysis conclude to an average of 67dB in the post anesthesia care unit. No many studies were reported about noise impact in a post-anesthesia care unit. Only one was published by B.Allaouchiche in 2002. However, noise is a complaint reported by patients and it could be responsible for physiological and psychological troubles. In this prospective study, the main objective is to determine patients' satisfaction in the post anesthesia care unit, before and after installation of a noise warning device. Between the two parts, a short training about noise consequences on health will be presented to nurses. Improvement off anti-noise actions on patient's satisfaction will analysed.

Detailed Description

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Although the post- anesthesia care unit can be noisy, the effect of noise on patients recovering from anesthesia is unknown. Indeed, many studies are achieved in reanimation or ICU. That's why this prospective study is about patients' satisfaction after their stay in the post-anesthesia care unit. In a first part, noise is just measured with a sound level meter and patients are asked about their experience. Before the second part, during few days, nurses will be informed about noise consequences on heath. With some precaution, a decrease of the sound level in a room (ex: decrease scope alarms, speaking quietly, not slamming the drawer, noise warning device…) will be expected. The main objective is to determine the patient's satisfaction in the post-anesthesia care unit before and after installation of a noise warning device.

Conditions

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All Surgery

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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before nurses formation/installation of a noise warning device

ambulatory or hospitalized patients, who go in post-anesthesia care unit, before nurses formation and installation of a noise warning device

questionnaire

Intervention Type OTHER

questionnaire EVAN-G

after nurses formation/installation of a noise warning device

ambulatory or hospitalized patients, who go in post-anesthesia care unit, after nurses formation and installation of a noise warning device

questionnaire

Intervention Type OTHER

questionnaire EVAN-G

Interventions

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questionnaire

questionnaire EVAN-G

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* patient who have a scheduled surgery in University hospital of Reims
* patient who stay in the post-anesthesia care unit
* patient consenting to participate to the study
* patient older than 18 years

Exclusion Criteria

* Emergency surgery
* Patients who have been hearing disorders (notice in the preoperative consultation)
* Patients who have cognitive disorders (notice in the preoperative consultation)
* Patients who have a medical history of ear/cerebral surgery
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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CHU de Reims

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Chu Reims

Reims, , France

Site Status

Countries

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France

Other Identifiers

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PO18016

Identifier Type: -

Identifier Source: org_study_id

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