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NCT05134155 Clinical Trial

A Pilot Study to Test the Acceptability and Feasibility of Relaxation Rooms to Help Reduce Occupational Stress Among Healthcare Workers

Stress Clinical Trial

Official title:
A Pilot Study to Test the Acceptability and Feasibility of Relaxation Rooms to Help Reduce Occupational Stress Among Healthcare Workers

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05134155
Other study ID # 21-002545
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 26, 2022
Est. completion date October 27, 2022

Study information
Verified date March 2023
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 86
Est. completion date October 27, 2022
Est. primary completion date October 27, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Clinician at Mayo working at St. Mary's hospital or the downtown Rochester campus during the study Exclusion Criteria: - 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (2)
Lead Sponsor Collaborator
Mayo Clinic Well Living Lab, Inc.

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Acceptability the proportion of clinicians who found the MindBreaks room to be somewhat acceptable or acceptable 12 months
Secondary Recruitment the number recruited 12 months
Secondary Room Usage how long participants stayed in the MindBreaks room 12 months
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