NCT05134155

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
86

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Feb 2022

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 14, 2021

Completed
10 days until next milestone

First Posted

Study publicly available on registry

November 24, 2021

Completed
3 months until next milestone

Study Start

First participant enrolled

February 26, 2022

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 27, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 27, 2022

Completed
Last Updated

March 16, 2023

Status Verified

March 1, 2023

Enrollment Period

8 months

First QC Date

November 14, 2021

Last Update Submit

March 14, 2023

Conditions

Burn OutStress

Outcome Measures

Primary Outcomes (1)

  • Acceptability

    the proportion of clinicians who found the MindBreaks room to be somewhat acceptable or acceptable

    12 months

Secondary Outcomes (2)

  • Recruitment

    12 months

  • Room Usage

    12 months

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Only clinicians at Mayo will be recruited as part of this study.

You may qualify if:

  • Clinician at Mayo working at St. Mary's hospital or the downtown Rochester campus during the study

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mayo Clinic in Rochester

Rochester, Minnesota, 55905, United States

Location

Related Links

MeSH Terms

Conditions

Burnout, Psychological

Condition Hierarchy (Ancestors)

Stress, PsychologicalBehavioral SymptomsBehavior

Study Officials

  • Liselotte N Dyrbye, MD, MHPE

    Mayo Clinic

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Medicine

Study Record Dates

First Submitted

November 14, 2021

First Posted

November 24, 2021

Study Start

February 26, 2022

Primary Completion

October 27, 2022

Study Completion

October 27, 2022

Last Updated

March 16, 2023

Record last verified: 2023-03

Locations

US(1)