Predicting Burnout in Nurses

Sponsor
Mayo Clinic (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05481138
Collaborator
National Institute of Nursing Research (NINR) (NIH)
360
2
40.6
180
4.4

Study Details

Study Description

Brief Summary

The purpose of this study is to develop a technology to predict burnout in RNs by measuring workplace, psychological, and physiological factors experienced by nurses.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    360 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Wearable Augmented Prediction of Burnout in Nurses: A Synergy of Engineering, Bioethics, Nursing and Wellness Sciences
    Actual Study Start Date :
    Aug 15, 2022
    Anticipated Primary Completion Date :
    Jan 1, 2026
    Anticipated Study Completion Date :
    Jan 1, 2026

    Outcome Measures

    Primary Outcome Measures

    1. Change in Maslach Burnout Inventory-Human Services Survey (MBI-HSS) [Baseline, 3 months, 6 months, 9 months, 12 months]

      Self-reported Maslach Burnout Inventory-Human Services Survey (MBI-HSS) assess clinician well-being in dimensions of burnout, engagement, and professional satisfaction. 22-item questionnaire ranking job-related feeling on 0 to 6 scale; 0 = never had this feeling, 6 = every day had this feeling

    Secondary Outcome Measures

    1. Change in Quick Inventory of Depressive Symptomatology (QIDS-SR) [Baseline, 3 months, 6 months, 9 months, 12 months]

      Self-reported Quick Inventory of Depressive Symptomatology (QIDS-SR) is a 16-item questionnaire that rates depression symptoms over the past seven days on an individual question scale of 0 to 3. Total scores range from 0 to 27 with higher scores indicating greater severity of depressive symptoms.

    2. Change in LASA Quality of Life Scale [Baseline, 3 months, 6 months, 9 months, 12 months]

      Linear Analogue Self-Assessment (LASA) 6-item questionnaire that assess feelings during the past week on an individual question scale of 0 to 10; 0 = as bad as it can be, 10 = as good as it can be. Total scores range 6-60 with higher scores indicating better perception of quality of life.

    3. Sense of belonging [Baseline]

      Measured using a 2- item self-reported questionnaire on sense of belonging to the nursing unit and hospital on an individual question scale of 0 to 4; 0=no opinion, 4=very strong. Total scores range from 0 to 8 with higher score indicating a greater sense of belonging.

    4. Change in Food Intake Questionnaire [Baseline, 3 months, 6 months, 9 months, 12 months]

      Measured using a self-reported multifactor food intake 16-item questionnaire that assess how many times per day, week or month subjects ate each food on a scale of never, 1-3 times last month, 1-2 times per week, 3-4 times per week, 5-6 times per week, 1 time per day, 2 times per day, 3 times per day, 4 or more times per day

    5. Sleep quality [Every day over 12-month study period]

      Measures by smartwatch that is worn daily by the subject reported in hours of sleep

    6. Daily heart rate [12 months]

      Measured by smartwatch that is worn daily by the subject reported in beats per minute

    7. Daily physical activity [12 months]

      Measured by smartwatch that is worn daily by the subject reported in time spent in activity (minutes)

    8. Daily step count [12 months]

      Measured by smartwatch that is worn daily by the subject reported in number of steps per day

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 62 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Employed as a registered nurse at Mayo Clinic Rochester or Mayo Clinic Florida.

    • Primary work assignment is one of the following: medical-surgical units, operating and recovery rooms, emergency room, intensive/cardiac care units, or other special care units (including neonatal intensive care units and newborn nurseries).

    • Proficient in written and spoken English.

    • Able to provide written informed consent.

    Exclusion Criteria:
    • Any exception to above criteria.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mayo Clinic in Florida Jacksonville Florida United States 32224
    2 Mayo Clinic in Rochester Rochester Minnesota United States 55905

    Sponsors and Collaborators

    • Mayo Clinic
    • National Institute of Nursing Research (NINR)

    Investigators

    • Principal Investigator: William Bobo, MD, Mayo Clinic

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    William V. Bobo, M.D., Principal Investigator, Mayo Clinic
    ClinicalTrials.gov Identifier:
    NCT05481138
    Other Study ID Numbers:
    • 22-000447
    • R01NR020362-01
    First Posted:
    Aug 1, 2022
    Last Update Posted:
    Aug 18, 2022
    Last Verified:
    Aug 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by William V. Bobo, M.D., Principal Investigator, Mayo Clinic
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 18, 2022