NCT06343584

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
6

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jul 2021

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2021

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

April 27, 2022

Completed
9 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 6, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 6, 2022

Completed
1.9 years until next milestone

First Posted

Study publicly available on registry

April 2, 2024

Completed
Last Updated

March 23, 2026

Status Verified

April 1, 2022

Enrollment Period

10 months

First QC Date

April 27, 2022

Last Update Submit

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

Other: Study will conducted over a six-month period using a quasi-experimental Pre-test/Post-test design using Stamm's (2009) ProQOL Scale.

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).

Other: Study will conducted over a six-month period using a quasi-experimental Pre-test/Post-test design using Stamm's (2009) ProQOL Scale.

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.

Group 1Group 2

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-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

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

Location

MeSH Terms

Conditions

Burnout, Psychological

Condition Hierarchy (Ancestors)

Stress, PsychologicalBehavioral SymptomsBehavior

Study Officials

  • Brooks Williams, DNP

    Methodist Health System

    PRINCIPAL INVESTIGATOR

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

Locations