The Impact of the MUSE Meditation Device on Student Registered Nurse Anesthetists

D

Diana J. Kelm

Status

Completed

Conditions

Burnout, Professional
Affect
Anxiety
Stress

Treatments

Device: MUSE Meditation Device

Study type

Interventional

Funder types

Other

Identifiers

NCT03839407
18-011173

Details and patient eligibility

About

The question this study is designed to answer is whether or not the use of a MUSE Meditation Device lowers student registered nurse anesthetist's perception of stress, anxiety, and burnout within the Mayo Clinic Doctorate of Nurse Anesthesia Practice Program.

Enrollment

34 patients

Sex

All

Ages

24 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

* Student Registered Nurse Anesthetists at Mayo Clinic in the class of 2021 and 2022.

Exclusion criteria

* Student Registered Nurse Anesthetists at Mayo Clinic who are not in the class of 2021 and 2022.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

34 participants in 4 patient groups

MUSE device Class 21
Experimental group
Description:
Participants will utilize the MUSE device for 12 weeks during the intervention period.
Treatment:
Device: MUSE Meditation Device
No MUSE device Class 21
No Intervention group
Description:
Participants will not utilize the MUSE device for 12 weeks during the non-intervention period.
MUSE device Class 22
Experimental group
Description:
Participants will utilize the MUSE device for 12 weeks during the intervention period.
Treatment:
Device: MUSE Meditation Device
No MUSE device Class 22
No Intervention group
Description:
Participants will not utilize the MUSE device for 12 weeks during the non-intervention period.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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