Clinical Trials Directory

Trials / Completed

CompletedNCT06343584

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

Status
Completed
Phase
Study type
Observational
Enrollment
6 (actual)
Sponsor
Methodist Health System · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

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.

Conditions

Interventions

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

Timeline

Start date
2021-07-01
Primary completion
2022-05-06
Completion
2022-05-06
First posted
2024-04-02
Last updated
2026-03-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06343584. Inclusion in this directory is not an endorsement.