The Impact of the MUSE Meditation Device on Student Registered Nurse Anesthetists
NCT ID: NCT03839407
Last Updated: 2021-04-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
34 participants
INTERVENTIONAL
2019-02-20
2021-02-23
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effects of Meditation on Stress and Fatigue
NCT06518031
A Study Of Resilience And Mental Well-Being Through Breathing Practice For Clinical Care Professionals
NCT07218458
Progressive Muscle Relaxation in Nursing Students: Effects on Psychological and Biopsychosocial Outcomes
NCT07038109
Meditation for Burnout in PA Students
NCT04169724
Student Stress Levels and Management Through Meditation
NCT02821611
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
SUPPORTIVE_CARE
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
MUSE device Class 21
Participants will utilize the MUSE device for 12 weeks during the intervention period.
MUSE Meditation Device
The MUSE Meditation Device guides users in mindful meditation using real-time feedback on brain wave activity.
No MUSE device Class 21
Participants will not utilize the MUSE device for 12 weeks during the non-intervention period.
No interventions assigned to this group
MUSE device Class 22
Participants will utilize the MUSE device for 12 weeks during the intervention period.
MUSE Meditation Device
The MUSE Meditation Device guides users in mindful meditation using real-time feedback on brain wave activity.
No MUSE device Class 22
Participants will not utilize the MUSE device for 12 weeks during the non-intervention period.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
MUSE Meditation Device
The MUSE Meditation Device guides users in mindful meditation using real-time feedback on brain wave activity.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
24 Years
55 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Diana J. Kelm
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Diana J. Kelm
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Diana Kelm, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Mayo Clinic
Rochester, Minnesota, United States
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
Mayo Clinic Clinical Trials
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
18-011173
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.