The Effects of Background Noise for Adult Patients' Sleep Quality in Intensive Care Unit.

Sponsor
Chang Gung Memorial Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05785130
Collaborator
Kaohsiung Medical University (Other)
70
1
2
24
2.9

Study Details

Study Description

Brief Summary

Poor sleep quality is one of the most common problems among adult patients in the intensive care unit (ICU). The causes of sleep disturbance are complicated. Poor sleep quality can lead to negative consequences for patients' physical and mental health. Non-pharmacological interventions, such as background noise, have been recommended to increase the threshold level of sound during nighttime and achieve masking effects to improve subjective sleep quality. This study is a randomized controlled trial that compared two parallel patient groups.The hypothesis of this study is that background noise can improve sleep quality in adult ICU patients compared with conventional treatment group.

Condition or Disease Intervention/Treatment Phase
  • Other: background noise
N/A

Detailed Description

Poor sleep quality is one of the most common problems among adult patients in the intensive care unit (ICU). Statistics indicate that over 50% of ICU patients report sleep abnormalities, such as sleep fragmentation, arousals, frequent awakenings, and poor sleep quality. The causes of sleep disturbance are complicated, with evidence suggesting that environmental factors such as noise, from alarms and machines that are active around the clock in the ICU, play a significant role. Poor sleep quality can lead to negative consequences for patients' physical and mental health.

Sleep promotion interventions, including both pharmacological and non-pharmacological approaches, have been proposed. However, the side effects of pharmacological intervention may also lead to poor outcomes. Therefore, non-pharmacological interventions, such as background noise, have been recommended to increase the threshold level of sound during nighttime and achieve masking effects to improve subjective sleep quality.

This study was conducted in randomized controlled trial that compared two parallel patient groups. Patients were included by convenience sampling in a medical center in Taiwan. The Verran and Snyder-Halpern Sleep Scale (VSHSS) was used to assess subjective sleep quality. The main purpose of this study was to investigate the effect of background noise intervention in sleep quality in adult intensive care unit patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
The Effects of Background Noise for Adult Patients' Sleep Quality in Intensive Care Unit: a Randomized Controlled Trial
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Mar 1, 2025
Anticipated Study Completion Date :
Mar 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: background noise group

Background noise at bedtime.

Other: background noise
Using sound machine for 3 days at bedtime for 7 hours(11p.m.- 6a.m.) in a decibel of 40-50.

No Intervention: conventional treatment group

Treatment as usual.

Outcome Measures

Primary Outcome Measures

  1. The Verran and Snyder-Halpern Sleep Scale scores changed from baseline to 1st days, 3rd days and 5th days. [Baseline, 1st days, 3rd days and 5th days.]

    Sleep quality is accessed by using Verran and Snyder-Halpern(VSH) Sleep Scale, a subjective sleep scale contains three dimensions: sleep disturbance, sleep effectiveness and sleep supplementation with totally 15 items. Scores were measured by using visual analogue scale which is a 100mm horizontal lines. The maxium score is 100 and the minimum score is 0. Totally score of VSHSS range from 0 to 1500. The lower of the score, the poorer of the sleep quality.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age must be greater than or equal to 20 years old.

  • Admitted to the ICU and have been intubated for at least 24 hours.

  • Aware of people, time, and place, and without hearing impairment.

  • Be able to communicate in writing.

  • The Glasgow Coma Scale score must be equal to or greater than 11, with a vocal response of 1 in the patient post-endotracheal tube placement.

Exclusion Criteria:
  • History of insomnia, Alzheimer's disease, or depression.

  • Routine use of sedative-hypnotic drugs (opioids, benzodiazepines, non-benzodiazepines, antihistamines, and melatonin) before admission.

  • Post-operation in the operating room before ICU admission.

  • ICDSC score of at least 4 or CAM-ICU positive.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Chang Gung Memorial Hospital Kaohsiung city Taiwan 833401

Sponsors and Collaborators

  • Chang Gung Memorial Hospital
  • Kaohsiung Medical University

Investigators

  • Principal Investigator: Ya-Ching Nien, Chang Gung Memorial Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ya-Ching, Nien, Principal Investigator, Chang Gung Memorial Hospital
ClinicalTrials.gov Identifier:
NCT05785130
Other Study ID Numbers:
  • 202300153B0
First Posted:
Mar 27, 2023
Last Update Posted:
Mar 29, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ya-Ching, Nien, Principal Investigator, Chang Gung Memorial Hospital

Study Results

No Results Posted as of Mar 29, 2023