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NCT Number: NCT06875882

Evaluating Occupational Stress in Surgeons and Musicians: A Multi-modal Pilot Study Using Wearable EEG, Biomarker Analysis and Validated Questionnaires

To learn about occupational stress among surgeons and musicians by integrating psychological assessments, neurophysiological measures, and biomarkers.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

MD Anderson Cancer Center

Houston, Texas, 77030, United States

Location status: Recruiting

Location contact

Mei Rui, DMA

CONTACT

[email protected]

713-597-1690

About this study

Primary Objectives • To assess the change in occupational stress among surgeons and musicians by measuring physiological and psychological stress markers.

Endpoints:

  • Changes in salivary cortisol levels (before and after surgeries for surgeons and live public performances for musicians).
  • Changes in State-Trait Anxiety Inventory-Short (STAI-S) scores (administered pre- and post-surgery/performance).

SECONDARY OBJECTIVES AND ENDPOINTS

  • Assessing and comparing anxiety and burnout, based on the MBI, STAI-T, M-PAS, and SCAT, in surgeons and musicians

Endpoints:

  • Baseline levels of anxiety and burnout measured using the MBI, M-PAS, STAI-T, and SCAT.
  • Emotional exhaustion, depersonalization, and personal accomplishment from the MBI in both groups.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Adults aged 18 years and older
  • Professional musicians (i.e., those with academic or orchestral appointments) or MD Anderson Neurosurgeons
  • For Musicians only: You will have a musical performance within three months of study enrollment.

For Neurosurgeons only: You will perform a surgical procedure within three months of study enrollment.

Exclusion criteria

  • Individuals who are unable to provide informed consent
  • Individuals diagnosed with severe cognitive impairments, severe psychiatric disorders, or hearing or visual impairments that could affect participation
  • Individuals previously enrolled in the study
  • Non-English-speaking musicians and/or surgeons

Treatment and study plan

Occupational Stress in Surgeons and Musicians

Behavioral

Participants will complete 5 questionnaires about participants demographics, burnout rates, and anxiety levels after participants consent to this study. These questionnaires will be sent to participants via email and should take about 15-20 minutes to complete.

Primary outcomes

  1. Safety and Adverse Events (AEs).

    Time frame: Through study completion; an average of 1 year.

Study contacts

Contact information is provided by the study sponsor or research team.

Mei Rui, DMA

CONTACT

[email protected]

(713) 597-1690

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Registry information

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Mar 13, 2025
Registry last updated
Apr 15, 2026

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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