RECRUITING

Work Time Schedule Changes for Nurse Managers

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to explore how working a 4-day schedule impacts nurse manager wellbeing and job performance. The main questions it aims to answer are: * Do those working 4-days have improved wellbeing with reduced levels of burnout and work/family conflict when compared to those in the control group? * Do levels of sleep, heart rate variability, and physical activity significantly differ between those working the 4-day schedule change and those in the control group? * Are nurse manager satisfaction, patient satisfaction, and patient quality outcomes different among those working the 4-day schedule change and those in the control group? Researchers will compare those working the 4-day schedule change to those working the standard 5-day schedule to determine causality between the intervention and the outcomes. Participants will: * Complete an initial visit to learn about the study. * Begin wearing an OURA ring, which will collect data on physical activity, sleep, and heart rate variability. They will need to download the Oura Ring app on their phone and log in weekly to sync data so that the researchers may access it. * Complete the first survey on the online REDCap platform (baseline). * Begin the work schedule that was assigned to them. * Clock in and out of work each shift. * Take the follow-up survey online (month 3). * Take the final survey online (month 6).

Official Title

Measuring the Effects of Potential Work Time Schedule Changes on Nurse Manager Health and Patient Outcomes

Quick Facts

Study Start:2025-01
Study Completion:2025-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06406478

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 18 years old or older
  2. * Registered nurse
  3. * Currently employed as a full-time nurse manager
  4. * Having a span of control greater than 40 Full Time Equivalent (FTE) Direct Reports
  5. * Currently working at either Ronald Regan UCLA Medical Center or UCLA Medical Center Santa Monica
  6. * In the acute care setting
  1. * Those working in ambulatory care settings
  2. * Nurse leaders with less than 30 FTE's
  3. * Working part time
  4. * Working a schedule less than 5 days a week

Contacts and Locations

Study Contact

Elizabeth G Keller, PhD
CONTACT
8593915038
kellere4@g.ucla.edu
Jian Li, MD, PhD
CONTACT
310-206-3788
JiaLi@mednet.ucla.edu

Principal Investigator

Jian Li, MD, PhD
PRINCIPAL_INVESTIGATOR
University of California, Los Angeles

Study Locations (Sites)

Ronald Reagan UCLA Medical Center
Los Angeles, California, 90095
United States
UCLA Health, Santa Monica
Santa Monica, California, 90404
United States

Collaborators and Investigators

Sponsor: University of California, Los Angeles

  • Jian Li, MD, PhD, PRINCIPAL_INVESTIGATOR, University of California, Los Angeles

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-01
Study Completion Date2025-09

Study Record Updates

Study Start Date2025-01
Study Completion Date2025-09

Terms related to this study

Additional Relevant MeSH Terms

  • Work-Related Condition