Creating Naptime: An Overnight, Non-Pharmacologic Intensive Care Unit Sleep Promotion Protocol

Sleep Clinical Trial

Official title: Creating Naptime: An Overnight, Non-Pharmacologic Intensive Care Unit Sleep Promotion Protocol

Status Completed

Clinical Trial Summary

Specific Aims:

1. Quantify baseline patient room disruptions in the medical ICU during the proposed nocturnal Naptime .

1. Obtain baseline light and noise levels in selected medical ICU study rooms.

2. Obtain baseline activity level levels in selected medical ICU study rooms.

3. Assess baseline information regarding nursing experience, prior training / beliefs regarding sleep promotion in the medical ICU

2. Assess the feasibility of instituting a 4 hour (Midnight to 4:00 AM) nocturnal Naptime with minimization of patient interaction via tracking of differences in patient room activity, light and noise levels in control versus intervention patients.

Secondary Aim

3. Examine the associations between Naptime provision and patient sleep quality.

Clinical Trial Description

The effects of poor sleep are dauntingly pleiotropic. Inasmuch as sleep deprivation can behaviorally and physiologically mimic delirium in the ICU, there is concern that sleep deprived ICU patients are at risk for the increased mortality, longer hospital stays and worsened physical and mental outcomes of hospitalized patients who experience delirium during their admission. Furthermore, lack of sleep has been associated with decrements in FEV1, FVC and maximal inspiratory pressure in non-ICU COPD patients, increases in respiratory muscle fatigue in healthy volunteers and blunted response to hypercapnea in healthy volunteers. Finally, theoretical concerns exist regarding sleep loss putting patients at risk for prolonged bedrest, adverse cardiovascular events, derangement of metabolism and endocrine function as well as immune suppression; though supported by animal models and brief studies in healthy volunteers, no ICU data exists. ;

Related Conditions & MeSH terms

• Sleep

• NCT number: NCT03119207
• Study type: Interventional
• Source: Yale University
• Status: Completed
• Phase: N/A
• Start date: November 4, 2012
• Completion date: June 22, 2014