Napping Rooms + Light Blocking Glasses for Burnout
Trial Summary
Will I have to stop taking my current medications?
The trial requires that you stop using prescription or over-the-counter sleep aids, including melatonin. Other medications are not mentioned, so it's unclear if you need to stop them.
What data supports the effectiveness of the treatment involving access to napping/relaxation rooms and blue and green light blocking glasses for burnout?
Is it safe for humans to use napping rooms and light-blocking glasses?
How does the treatment of napping rooms and light blocking glasses for burnout differ from other treatments?
This treatment is unique because it combines access to a napping room with the use of blue and green light blocking glasses, which may help regulate the body's internal clock and improve sleep quality. Unlike traditional treatments for burnout that might focus on stress management or medication, this approach targets sleep and light exposure to potentially enhance rest and recovery.6791011
What is the purpose of this trial?
Healthy and happy nurses are essential to ensuring optimal patient outcomes and organizational success. The evidence on the negative impacts of night shift on nurses' health and cognitive function, and their implications on patient outcomes and organizational costs, reflect the need for interventions to mitigate these detrimental outcomes.This pilot, feasibility, clinical trial will examine the feasibility of two fatigue countermeasure interventions (access to napping/relaxation room and use of blue/green light blocking glass during night shift) and explore the interventions effects on nurses' health, missed care, and burnout.
Eligibility Criteria
This trial is for night shift nurses who are experiencing burnout or want to maintain their health. Participants should be currently working night shifts and willing to try using a napping/relaxation room and blue/green light blocking glasses as part of the study.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Participants undergo fatigue countermeasure interventions including access to napping/relaxation room and use of blue/green light blocking glasses during night shift
Washout
A two-week washout period between different intervention conditions
Follow-up
Participants are monitored for changes in health, sleep, fatigue, cognitive function, and burnout after interventions
Treatment Details
Interventions
- Access to napping/relaxation room
- Blue and green light blocking glasses
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Pittsburgh
Lead Sponsor
Shadyside Hospital Foundation
Collaborator
Shadyside Hospital Foundation
Collaborator