Are Personal Smartphones Hurting Work-Life Balance for Nurse Managers?
1 other identifier
observational
6
1 country
1
Brief Summary
For leadership positions with only a handful of staff under their direct chain of command, this may not be all-consuming and detrimental to work-life balance. But for NMs with upwards of 100 direct reports, this can make for a never-ending stream of contact points. This study will implement several communication and behavioral strategies to determine how using provided smartphone tools impact work-life balance and professional burnout.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jul 2021
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2021
CompletedFirst Submitted
Initial submission to the registry
April 27, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 6, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
May 6, 2022
CompletedFirst Posted
Study publicly available on registry
April 2, 2024
CompletedMarch 23, 2026
April 1, 2022
10 months
April 27, 2022
March 19, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
• Impact of smartphone tool utilization will be measured using a pre-study survey and post-study survey using the Professional Quality of Life (ProQOL) Scale (Stamm, 2009).
• Impact of smartphone tool utilization will be measured using a pre-study survey and post-study survey using the Professional Quality of Life (ProQOL) Scale (Stamm, 2009).
6 months
Secondary Outcomes (4)
• Participants in Group 1 will self-report on the post-study survey (Appendix D1) the number of tools implemented during the study duration.
6 months
• Participants in Group 1 will self-report on the post-study survey (Appendix D1) the frequency of tool utilization during the study duration using a Likert scale.
6 months
• Participants in Group 2 will self-report on the post-study survey (Appendix D2) using the ProQOL Scale.
6 months
• Responses to the post-study survey from participants in Group 2 will be compared to participants in Group 1 to determine if utilizing a separate work smartphone during business hours has a greater improvement on work-life balance and burnout.
6 months
Study Arms (2)
Group 1
Must hold the title of Nurse Manager or Interim Nurse Manager at Methodist Mansfield Medical Center. Upon receipt of informed consent, participants will be divided into two groups. Group 1 will receive a list of suggested tools used to decrease the amount of smartphone interruptions after business hours
Group 2
Must hold the title of Nurse Manager or Interim Nurse Manager at Methodist Mansfield Medical Center. Upon receipt of informed consent, participants will be divided into two groups. Group 2 will receive a work-issued smartphone with instructions for use (Appendix C).
Interventions
Group 1 will receive a list of suggested tools used to decrease the amount of smartphone interruptions after business hours (Appendix B) and Group 2 will receive a work-issued smartphone with instructions for use (Appendix C). Both groups will use a pre-post test format designed to compare the outcomes between the two groups. Post-study analysis will compare pre- and post-tests within each group and will compare Group 1 and Group 2 post-intervention outcomes.
Eligibility Criteria
* Participant must hold the title of Nurse Manager or Interim Nurse Manager at Methodist Mansfield Medical Center * Participant must have greater than 50 direct reports
You may qualify if:
- Participant must hold the title of Nurse Manager or Interim Nurse Manager at Methodist Mansfield Medical Center
- Participant must have greater than 50 direct reports
You may not qualify if:
- Participant expects to separate employment with Methodist Health System prior to the conclusion of the study
- Participant does not use their personal smartphone to communicate with direct reports
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Methodist Mansfield Medical Center
Mansfield, Texas, 76063, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Brooks Williams, DNP
Methodist Health System
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 27, 2022
First Posted
April 2, 2024
Study Start
July 1, 2021
Primary Completion
May 6, 2022
Study Completion
May 6, 2022
Last Updated
March 23, 2026
Record last verified: 2022-04