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

NCT03119207 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 85

Last updated 2017-04-18

No results posted yet for this study

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.

Conditions

  • Sleep

Interventions

BEHAVIORAL

Naptime Protocol

Between midnight and 4:00 every attempt will be made to limit staff entrance into the patient room.

Sponsors & Collaborators

  • National Institute of Nursing Research (NINR)

    collaborator NIH

  • Yale University

    lead OTHER

Principal Investigators

  • Melissa Knauert, MD, PhD · Yale University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-11-04
Primary Completion
2014-06-22
Completion
2014-06-22

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03119207 on ClinicalTrials.gov