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Completed

NCT Number: NCT03839407

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

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.

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Key information

Conditions

Stress Affect Anxiety Anxiety Disorders Behavior Behavioral Symptoms Burnout, Professional Burnout, Psychological Mental Disorders Occupational Diseases Occupational Stress Stress, Psychological

Age range

24 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Clinic

Rochester, Minnesota, 55905, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

MUSE Meditation Device

Device

The MUSE Meditation Device guides users in mindful meditation using real-time feedback on brain wave activity.

Primary outcomes

  1. Change in Stress, as measured by the Perceived Stress Scale-10

    Time frame: baseline and 3, 6, and 12 months

    Scores range from 0 to 40 with 0 indicating no stress and a higher score indicating greater stress.

Secondary outcomes

  1. Change in Anxiety, as measured by the Generalized Anxiety Disorder Scale-7

    Time frame: baseline and 3, 6, and 12 months

    Scores range from 0 to 21 with 0 indicating no anxiety and a higher score indicating greater anxiety.

  2. Change in Affect, as measured by the Positive and Negative Affect Scale

    Time frame: baseline and 3, 6, and 12 months

    Scores range from 10-50 within positive and negative scales. The higher the score, the higher the positive or negative affect.

  3. Change in Burnout, as measured by the Maslach Burnout Inventory-2

    Time frame: baseline and 3, 6, and 12 months

    A two question survey asking the participant burnout questions within the workplace.

  4. Change in Self-Perceived Medical Error, as measured by a single question.

    Time frame: 3 & 6 months

    A single yes or no question asking if participant felt they made any medical errors

Sponsors and collaborators

Lead sponsor

Diana J. Kelm

Other

Registry information

Official study title

The Impact of the MUSE Meditation Device on Perceived Stress, Anxiety, Affect, and Burnout Among Student Registered Nurse Anesthetists

Acronym: MUSE

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Feb 15, 2019
Registry last updated
Apr 8, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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