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N/A N=40 Supportive Care

A Study to Asses Wellness Using a Brain Sensing Device on Physicians

Stress, Emotional · Sleep · Quality of Life

Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Dec 2024
Primary outcome: Primary: Frequency Adherence to Intervention — 57.8 times used

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Muse S™ Headband system (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Mayo Clinic
Primary completion
Aug 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Frequency Adherence to Intervention
57.8
PRIMARY
Duration Adherence to Intervention
5.9
SECONDARY
Perceived Stress Scale (PSS) Score Difference
-2.1
SECONDARY
Resilience Score Difference
1.4
SECONDARY
LASA Score Difference
2.7

Summary

A study to asses the feasibility of physicians using a wearable brain sensing wellness device during a time of increased work load, patient volume and stressors to assess the association between duration of active state and calm state as measured by the wearable brain sensing wellness device, and quality of life (QOL), subjective stress, sleep and resilience.

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older at time of consent
  • Practicing Physicians at Mayo Clinic
  • Not pregnant by subject self-report at time of consent
  • Have the ability to provide informed consent
  • Have the ability to complete all aspects of this trial
  • Have access to a smart phone or tablet device
  • Have no contraindicating comorbid health condition which would interfere with the proper use of the Muse-S™ system, as determined by the clinical investigators

Exclusion Criteria

  • Used an investigational drug within the past 30 days
  • Currently (within the past 3 weeks) been practicing mindfulness training on a weekly/regular basis
  • Currently (within 3 weeks) been enrolled in another clinical or research program (e.g. CAM) which intervenes on the patients' QOL, or stress
  • An unstable medical or mental health condition as determined by the physician investigator
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04743973). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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