Are Personal Smartphones Hurting Work-Life Balance for Nurse Managers?

March 19, 2026 updated by: Methodist Health System
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.

Study Overview

Detailed Description

The study will be conducted over a six-month period using a quasi-experimental Pre-test/Post-test design using Stamm's (2009) ProQOL Scale. This study is being done as a pilot study with a small sample size. NMs will be recruited as volunteers for participation in the study with an anticipated six-month time commitment. 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 (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.

Study Type

Observational

Enrollment (Actual)

6

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Mansfield, Texas, United States, 76063
        • Methodist Mansfield Medical Center

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.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

  • 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

Description

Inclusion 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

Exclusion Criteria:

  • 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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
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 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.
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).

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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
• 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).
Time Frame: 6 months
• 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 Outcome Measures

Outcome Measure
Measure Description
Time Frame
• Participants in Group 1 will self-report on the post-study survey (Appendix D1) the number of tools implemented during the study duration.
Time Frame: 6 months
• 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.
Time Frame: 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.
Time Frame: 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.
Time Frame: 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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Brooks Williams, DNP, Methodist Health System

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 Major Dates

Study Start (Actual)

July 1, 2021

Primary Completion (Actual)

May 6, 2022

Study Completion (Actual)

May 6, 2022

Study Registration Dates

First Submitted

April 27, 2022

First Submitted That Met QC Criteria

March 26, 2024

First Posted (Actual)

April 2, 2024

Study Record Updates

Last Update Posted (Actual)

March 23, 2026

Last Update Submitted That Met QC Criteria

March 19, 2026

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 023.NUR.2021.M

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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