Burn OutNCT05134155
A Pilot Study to Test the Acceptability and Feasibility of Relaxation Rooms to Help Reduce Occupational Stress Among Healthcare Workers
An observational study of Burn Out and Stress, run by Mayo Clinic at 1 site in United States.
Trial summary
Test the acceptability and feasibility of a relaxation room to reduce work stress among clinicians and collect clinician-reported outcome data after using the relaxation room. Read more about this study
- Who is it for?
- Ages 18 to 80 yearsHealthy volunteers can take part
- How many people
- 86 participants
- Where
- 1 siteUnited States
- Study dates
- 26 Feb 2022to 27 Oct 2022
- 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 18 to 80 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Only clinicians at Mayo will be recruited as part of this study.
Who may be able to join
- Clinician at Mayo working at St. Mary's hospital or the downtown Rochester campus during the study
Who cannot join
- Any physical condition that might prevent them from sitting for 20-30 minutes in the room
- Significant hearing loss that they would not be able to hear the audio stimuli
- Significant vision loss that they would not be able to see the visual stimuli
Trial locations and contacts
1 site in 1 country.
United States1 site
Mayo Clinic in Rochester
Rochester, Minnesota, 55905
About this study
Test the acceptability and feasibility of a relaxation room to reduce work stress among clinicians and collect clinician-reported outcome data after using the relaxation room.
Read the detailed description
The plan is to pilot test a relaxation room to demonstrate its acceptability and feasibility in the hospital and collect clinician-centered outcomes. This study will inform the design of a future trial using this intervention.
- Medical subject headings
- Burnout, Psychological
What is being measured
The primary outcome is the main question the study is designed to answer.
Acceptability
the proportion of clinicians who found the MindBreaks room to be somewhat acceptable or acceptable
Measured: 12 months
Secondary outcomes (2)
Recruitment
the number recruited
Measured: 12 months
Room Usage
how long participants stayed in the MindBreaks room
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 posted24 Nov 2021
- Study start26 Feb 2022
- Primary completion27 Oct 2022
- Study completion27 Oct 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Burn OutStudies 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
- 86 participants (actual)
Sponsor and investigators
- Lead sponsor
- Mayo Clinic
- Sponsor type
- University, hospital or other
- Collaborators
- Well Living Lab, Inc.
- Responsible party
- Principal investigator, Colin West, Mayo Clinic
- Investigators
- Liselotte N Dyrbye, MD, MHPE, Principal investigator, Mayo Clinic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05134155
- Sponsor's protocol ID
- 21-002545
- Status last verified
- Mar 2023
- First submitted
- 14 Nov 2021
- Last updated
- 16 Mar 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Mar 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Pilot Study to Test the Acceptability and Feasibility of Relaxation Rooms to Help Reduce Occupational Stress Among Healthcare Workers
- ClinicalTrials.gov ID
- NCT05134155
- Acronym / sponsor ID
- 21-002545
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 86 participants (actual)
- Lead sponsor
- Mayo ClinicUniversity, hospital or other
- Collaborators
- Well Living Lab, Inc.
- Study start
- 26 Feb 2022 (actual)
- Primary completion
- 27 Oct 2022 (actual)
- Study completion
- 27 Oct 2022 (actual)
- First posted
- 24 Nov 2021 (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.
Test the acceptability and feasibility of a relaxation room to reduce work stress among clinicians and collect clinician-reported outcome data after using the relaxation room.
Detailed description
The plan is to pilot test a relaxation room to demonstrate its acceptability and feasibility in the hospital and collect clinician-centered outcomes. This study will inform the design of a future trial using this intervention.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Only clinicians at Mayo will be recruited as part of this study.
Key inclusion criteria (1 listed)
- Clinician at Mayo working at St. Mary's hospital or the downtown Rochester campus during the study
Key exclusion criteria (3 listed)
- Any physical condition that might prevent them from sitting for 20-30 minutes in the room
- Significant hearing loss that they would not be able to hear the audio stimuli
- Significant vision loss that they would not be able to see the visual stimuli
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
Acceptability
Time frame: 12 months
the proportion of clinicians who found the MindBreaks room to be somewhat acceptable or acceptable
2 secondary outcomes
Recruitment
Time frame: 12 months
Room Usage
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 16 Mar 2023.
- Mayo Clinic Clinical TrialsLink provided by the sponsor.
Related trials for Burn Out
RecruitingObservational study
Early Maladaptive Schemas in French Health Care Professionals With Burn Out
Burn Out
Recruiting
Reducing Burnout in Healthcare Workers Through Yoga and Square Breathing Practices
Burn-Out
Not yet recruiting
Mitigating Burnout in Nursing and Associated Healthcare Staff
Burn Out, Nurses
Recruiting
Building Resilience at Schools: Emotional and Biological Assessment and Treatment of Traumatic Stress
Post Traumatic Stress Disorder, Complex Posttraumatic Stress Disorder
Recruiting
Creative Arts Program to Reduce Burnout in Healthcare Professionals
Burn-Out Syndrome, Post-Traumatic Stress Disorder
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.
Liselotte N Dyrbye, MD, MHPE principal investigator
Mayo Clinic
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Burn Out and Stress, run by Mayo Clinic at 1 site 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 1 inclusion and 3 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 16 Mar 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site 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?
Acceptability (time frame: 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 16 Mar 2023; AzTrials last refreshed its copy on 28 Oct 2026.