Burnout, Healthcare WorkersNCT05481138
Predicting Burnout in Nurses
An observational study of Burnout, Healthcare Workers, run by Mayo Clinic at 2 sites in United States.
Trial 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. Read more about this study
- Who is it for?
- Ages 20 to 62 yearsHealthy volunteers can take part
- Conditions the study is for
- Burnout, Healthcare Workers
- How many people
- 531 participants
- Where
- 2 sitesUnited States
- Study dates
- 15 Aug 2022to 1 Mar 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 20 to 62 years
- All sexes
- Healthy volunteers accepted
- Adult
Study population: Registered Nurses (RNs) at Mayo Clinic from Emergency Department, Intensive Care Units (including neonatal), selected Medical/Surgical units, and Inpatient Psychiatry. RNs from Inpatient Psychiatry will be recruited only from Mayo Rochester.
Who may be able to join
- 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.
Who cannot join
- Any exception to above criteria.
Trial locations and contacts
2 sites in 1 country.
United States2 sites
Mayo Clinic in Florida
Jacksonville, Florida, 32224
Mayo Clinic in Rochester
Rochester, Minnesota, 55905
About this study
Official title: Wearable Augmented Prediction of Burnout in Nurses: A Synergy of Engineering, Bioethics, Nursing and Wellness Sciences
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.
- Conditions
- Burnout, Healthcare Workers
- Keywords
- Registered Nurses, Artificial intelligence, Wearable
- Medical subject headings
- Burnout, Psychological
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Maslach Burnout Inventory-Human Services Survey (MBI-HSS)
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
Measured: Baseline, 3 months, 6 months, 9 months, 12 months
Secondary outcomes (8)
Change in Quick Inventory of Depressive Symptomatology (QIDS-SR)
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.
Measured: Baseline, 3 months, 6 months, 9 months, 12 months
Change in LASA Quality of Life Scale
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.
Measured: Baseline, 3 months, 6 months, 9 months, 12 months
Sense of belonging
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.
Measured: Baseline
Change in Food Intake Questionnaire
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
Measured: Baseline, 3 months, 6 months, 9 months, 12 months
Sleep quality
Measures by smartwatch that is worn daily by the subject reported in hours of sleep
Measured: Every day over 12-month study period
Daily heart rate
Measured by smartwatch that is worn daily by the subject reported in beats per minute
Measured: 12 months
Daily physical activity
Measured by smartwatch that is worn daily by the subject reported in time spent in activity (minutes)
Measured: 12 months
Daily step count
Measured by smartwatch that is worn daily by the subject reported in number of steps per day
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Aug 2022
- Study start15 Aug 2022
- Primary completion1 Jan 2025
- Study completion1 Mar 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Burnout, Healthcare WorkersStudies of the same condition, open and under way.
- More trials run by Mayo ClinicThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 531 participants (actual)
Sponsor and investigators
- Lead sponsor
- Mayo Clinic
- Sponsor type
- University, hospital or other
- Collaborators
- National Institute of Nursing Research (NINR)
- Responsible party
- Principal investigator, Arjun P. Athreya, Mayo Clinic
- Investigators
- Arjun P. Athreya, Ph.D., M.S., Principal investigator, Mayo Clinic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05481138
- Sponsor's protocol ID
- 22-000447
- Other IDs
- R01NR020362-01
- Status last verified
- Jun 2025
- First submitted
- 28 Jul 2022
- Last updated
- 24 Jun 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Wilton AR, Sheffield K, Wilkes Q, Chesak S, Pacyna J, Sharp R, Croarkin PE, Chauhan M, Dyrbye LN, Bobo WV, Athreya AP. The Burnout PRedictiOn Using Wearable aNd ArtIficial IntelligEnce (BROWNIE) study: a decentralized digital health protocol to predict burnout in registered nurses. BMC Nurs. 2024 Feb 13;23(1):114. doi: 10.1186/s12912-024-01711-8.
PubMed 38347557
Study at a glance
From the registry record, last updated by the sponsor on 24 Jun 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Wearable Augmented Prediction of Burnout in Nurses: A Synergy of Engineering, Bioethics, Nursing and Wellness Sciences
- ClinicalTrials.gov ID
- NCT05481138
- Acronym / sponsor ID
- 22-000447
- Conditions
- Burnout, Healthcare Workers
- Keywords
- Registered Nurses, Artificial intelligence, Wearable
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 531 participants (actual)
- Lead sponsor
- Mayo ClinicUniversity, hospital or other
- Collaborators
- National Institute of Nursing Research (NINR)
- Study start
- 15 Aug 2022 (actual)
- Primary completion
- 1 Jan 2025 (actual)
- Study completion
- 1 Mar 2025 (actual)
- First posted
- 1 Aug 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 20 to 62 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Registered Nurses (RNs) at Mayo Clinic from Emergency Department, Intensive Care Units (including neonatal), selected Medical/Surgical units, and Inpatient Psychiatry. RNs from Inpatient Psychiatry will be recruited only from Mayo Rochester.
Key inclusion criteria (4 listed)
- 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.
Key exclusion criteria (1 listed)
- Any exception to above criteria.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Change in Maslach Burnout Inventory-Human Services Survey (MBI-HSS)
Time frame: 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
8 secondary outcomes
Change in Quick Inventory of Depressive Symptomatology (QIDS-SR)
Time frame: Baseline, 3 months, 6 months, 9 months, 12 months
Change in LASA Quality of Life Scale
Time frame: Baseline, 3 months, 6 months, 9 months, 12 months
Sense of belonging
Time frame: Baseline
Change in Food Intake Questionnaire
Time frame: Baseline, 3 months, 6 months, 9 months, 12 months
Sleep quality
Time frame: Every day over 12-month study period
Daily heart rate
Time frame: 12 months
Daily physical activity
Time frame: 12 months
Daily step count
Time frame: 12 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jun 2025.
- Derived from this study: PubMed 38347557Wilton AR, Sheffield K, Wilkes Q, Chesak S, Pacyna J, Sharp R, Croarkin PE, Chauhan M, Dyrbye LN, Bobo WV, Athreya AP. The Burnout PRedictiOn Using Wearable aNd ArtIficial IntelligEnce (BROWNIE) study: a decentralized digital health protocol to predict burnout in registered nurses. BMC Nurs. 2024 Feb 13;23(1):114. doi: 10.1186/s12912-024-01711-8.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Arjun P. Athreya, Ph.D., M.S. principal investigator
Mayo Clinic
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Burnout, Healthcare Workers, run by Mayo Clinic at 2 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 24 Jun 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Maslach Burnout Inventory-Human Services Survey (MBI-HSS) (time frame: Baseline, 3 months, 6 months, 9 months, 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05481138, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2025.