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A Study on Noise Exposure Status and the Effect of Noise Management in Pediatric Intensive Care Unit

Primary Purpose

Noise Exposure, Delirium

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
noise management
Sponsored by
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Noise Exposure focused on measuring Noise Exposure, Delirium, pediatric, intensive care

Eligibility Criteria

undefined - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients aged ≤ 18 years
  • The predicted PICU LOS ≥12 hours
  • The informed consent of the child's guardian was obtained

Exclusion Criteria:

  • Patients with delirium on admission
  • Patients in a coma (Richmond Agitation Sedation Scale[RASS]-4 or -5) all through their stay in PICU
  • Patients with mental disorders or mental retardation, who continue to use antipsychotic drugs
  • Patients undergoing neurosurgery and neurology surgery
  • Hearing or visual impairment
  • Non Chinese or English language users
  • Missed or incomplete delirium score

Sites / Locations

  • Xinhua Hospital Affiliated To Shanghai Jiao Tong University School of MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

control group

experimental group

Arm Description

Patients in the control group will not receive any noise management intervention

Patients in the experimental group will receive noise management. The intervention measures mainly include the following three parts: control of noise source, control of noise transmission and personal protection of noise receiver.We will strengthen the education of medical staff to ensure the effective implementation of the noise management.

Outcomes

Primary Outcome Measures

Noise exposure
Noise is measured in decibels.The noise exposure in PICU will be described in Leq,Lmax,Lmin
Delirium incidence
Delirium screening is performed using the Cornell assessment of pediatric delirium(CAPD).Delirium will be screened every 12 hours(at 8:00a.m.&20:00p.m.) until the patient is transferred out of PICU or drops out

Secondary Outcome Measures

PICU length of stay(LOS)
PICU LOS is measured in days
Duration of mechanical ventilation(MV)
Duration of MV is measured in days
Hospital length of stay(LOS)
Hospital LOS is measured in days
Medical staff's knowledge of noise management
Medical staff's knowledge of noise management is evaluated by a self-made questionnaire

Full Information

First Posted
August 26, 2020
Last Updated
September 3, 2020
Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT04544085
Brief Title
A Study on Noise Exposure Status and the Effect of Noise Management in Pediatric Intensive Care Unit
Official Title
A Study on Noise Exposure Status and the Effect of Noise Management in Pediatric Intensive Care Unit
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
July 16, 2020 (Actual)
Primary Completion Date
November 2020 (Anticipated)
Study Completion Date
December 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study has two stages. At the first stage,the investigators will try to use noise detectors to investigate the status of noise exposure in the pediatric intensive care unit(PICU) and to analyze the main noise sources in it. At the second stage,the investigators will try to evaluate the effect of noise management on noise exposure and health outcomes of the pediatric patients in PICU.The investigators hypothesize that noise exposure in PICU is higher than the standard.The investigators also hypothesize that the implementation of the noise management will improve the noise exposure and health outcomes of the pediatric patients in PICU.
Detailed Description
This study has two stages. At the first stage,the investigators will try to use noise detectors to investigate the status of noise exposure in the pediatric intensive care unit(PICU) and to analyze the main noise sources in it. At the second stage,the investigators will try to evaluate the effect of noise management on noise exposure and health outcomes of the pediatric patients in PICU.The investigators hypothesize that noise exposure in PICU is higher than the standard.The investigators also hypothesize that the implementation of the noise management will improve the noise exposure and health outcomes of the pediatric patients in PICU. 1.For the investigation of the status of noise exposure: (1) Preparation of noise monitor equipment: select noise detectors conforming to the national standard. All noise detectors used in the study are of the same brand; (2) Use of noise monitor: set the mode of noise monitor according to the national standard: place the monitor in accordance with the requirements;(3) All the data of noise exposure will be collected and sorted out by the investigator. (4) Spss20.0 software is used for descriptive analysis and statistical inference. Mean ± standard deviation, median and quartile are used to describe measurement data, while frequency and percentage are used to describe counting data. Comparison between groups: when the measurement data obey normal distribution and the variance is homogeneous, two independent sample t-test are used to compare whether there is statistical difference between the two groups of indicators or index difference (measured value baseline value); if it does not obey normal distribution or the variance is uneven, non parametric statistical method is used; counting data: Chi square test is used to compare whether there is statistical difference between the two groups of index values, test level: α = 0.05 2.For the evaluation of the effect of noise management on noise exposure and health outcomes of the pediatric patients in PICU: (1)General information and clinical data of patients will be collected through hospital electronic information system, ICU nursing records, cases, doctor's advice and consultation. The investigator will evaluate and record the delirium score of ICU children who met the inclusion criteria each shift . At the time of discharge, PICU duration, hospital stay, MV duration and in-hospital mortality were inquired by EMR. (2) Quality control of intervention implementation are as follows:① According to the research results of early promotion strategy, relevant training materials were made to carry out training and education for PICU medical staff;② During the implementation of the intervention, irregular sampling of medical staff was conducted to evaluate the implementation of the intervention and give timely feedback.(3) Collection of information:① The data of patients will be collected by the investigator;② Pediatric delirium score: in order to ensure the quality of the study, the investigator will conduct random sampling and assess the delirium of children in the same patient with the nurses from time to time to investigate the evaluation quality;③ Input the data into EpiData, set reasonable numerical boundary value and logical check items. If there is logical error, check the original data for correction, and import the data into spss20.0 for statistical analysis. (4) Sample size assessment: the assessment of sample size in experimental research can also be divided into measurement data and counting data. The main outcome measures are delirium rate and noise exposure. Therefore, the incidence of delirium will be used as the rate to calculate the sample size.According to the calculation formula of the rate: n = (U α + U β) 22P (1-p) / (P1-P2) 2, the sample size of the control group and the intervention group are calculated. Uα=1.64,Uβ=0.84。P1 and P2 are the estimated values of delirium incidence before and after the intervention, and P is the total rate. The references showed that P1 = 33%, P2 = 14%.The sample size calculated by the formula is: (1.64 + 0.84) 2 * 2 * 0.47 * 0.53 / 0.192 = 85 cases, plus 20% of the sample loss, that is, 102 cases in the control group and 102 cases in the intervention group (5)Statistical Analysis:①Data set: use EpiData 3.1 software to establish the data set, and clean up and check the data;② The data will be imported into spss20.0 for statistical analysis. Descriptive analysis and statistical inference will be carried out. Mean ± standard deviation, median and quartile are used to describe measurement data, while frequency and percentage are used to describe counting data. Comparison between groups: when the measurement data obeys normal distribution and the variance is homogeneous, two independent sample t-test is used to compare whether there is statistical difference in the indicators or index difference (measured value baseline value) between the two groups; if the measurement data does not obey the normal distribution or the variance is uneven, non parametric statistical method is used; counting data: Chi square test is used to compare whether there is statistical difference between the two groups of patients Level: α = 0.05.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Noise Exposure, Delirium
Keywords
Noise Exposure, Delirium, pediatric, intensive care

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
204 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
control group
Arm Type
No Intervention
Arm Description
Patients in the control group will not receive any noise management intervention
Arm Title
experimental group
Arm Type
Experimental
Arm Description
Patients in the experimental group will receive noise management. The intervention measures mainly include the following three parts: control of noise source, control of noise transmission and personal protection of noise receiver.We will strengthen the education of medical staff to ensure the effective implementation of the noise management.
Intervention Type
Behavioral
Intervention Name(s)
noise management
Intervention Description
The intervention mainly includes the following three parts: control of noise source, control of noise transmission and personal protection of noise receiver.(1) control of noise source:equipment maintenance,alarm management,set quiet time,etc.;(2)control of noise transmission:improvement of architectural design;(3)personal protection of noise receiver:providing patients with earmuffs or earplugs.
Primary Outcome Measure Information:
Title
Noise exposure
Description
Noise is measured in decibels.The noise exposure in PICU will be described in Leq,Lmax,Lmin
Time Frame
Average of 1 weak
Title
Delirium incidence
Description
Delirium screening is performed using the Cornell assessment of pediatric delirium(CAPD).Delirium will be screened every 12 hours(at 8:00a.m.&20:00p.m.) until the patient is transferred out of PICU or drops out
Time Frame
Up to 1 month
Secondary Outcome Measure Information:
Title
PICU length of stay(LOS)
Description
PICU LOS is measured in days
Time Frame
60 days after the enrollment
Title
Duration of mechanical ventilation(MV)
Description
Duration of MV is measured in days
Time Frame
60 days after the enrollment
Title
Hospital length of stay(LOS)
Description
Hospital LOS is measured in days
Time Frame
60 days after the enrollment
Title
Medical staff's knowledge of noise management
Description
Medical staff's knowledge of noise management is evaluated by a self-made questionnaire
Time Frame
1 hour within the end of the lecture on noise management for medical staff

10. Eligibility

Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients aged ≤ 18 years The predicted PICU LOS ≥12 hours The informed consent of the child's guardian was obtained Exclusion Criteria: Patients with delirium on admission Patients in a coma (Richmond Agitation Sedation Scale[RASS]-4 or -5) all through their stay in PICU Patients with mental disorders or mental retardation, who continue to use antipsychotic drugs Patients undergoing neurosurgery and neurology surgery Hearing or visual impairment Non Chinese or English language users Missed or incomplete delirium score
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaohua Ge
Phone
+86-18616706778
Email
gexiaohua@shsmu.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaohua Ge
Organizational Affiliation
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Xinhua Hospital Affiliated To Shanghai Jiao Tong University School of Medicine
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200092
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaohua Ge
Phone
+86-21-25076124
Email
gexiaohua@shsmu.edu.cn

12. IPD Sharing Statement

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A Study on Noise Exposure Status and the Effect of Noise Management in Pediatric Intensive Care Unit

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