- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06343584
Are Personal Smartphones Hurting Work-Life Balance for Nurse Managers?
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Texas
-
Mansfield, Texas, United States, 76063
- Methodist Mansfield Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
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
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
Sponsor
Investigators
- Principal Investigator: Brooks Williams, DNP, Methodist Health System
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 023.NUR.2021.M
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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