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

NCT ID: NCT06875882

Last Updated: 2025-10-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-03-17

Study Completion Date

2028-03-31

Brief Summary

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

Detailed Description

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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.

Conditions

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Occupational Stress

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Occupational Stress

This research study is to learn about occupational stress among surgeons and musicians by integrating psychological assessments, neurophysiological measures, and biomarkers. Researchers want to assess and compare factors associated with occupational stress, among surgeons and musicians, such as changes in stress biomarkers before and after surgery or music performance, anxiety, burnout, demographic factors, and brainwave activity linked to stress. It is hoped the information learned in this study can be used to help promote better health outcomes and enhance the well-being of these workforce members. Participants will undergo saliva sample collections and complete questionnaires before and after the performance or surgery.

Occupational Stress in Surgeons and Musicians

Intervention Type 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.

Optional Procedure

Participants may optionally have a surgery or performance recorded and undergo an EEG while watching the recording. These participants will undergo saliva sample collections and complete questionnaires before and after the EEG recording session.

Occupational Stress in Surgeons and Musicians

Intervention Type 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.

Interventions

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Occupational Stress in Surgeons and Musicians

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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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M.D. Anderson Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mei Rui, DMA

Role: PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Locations

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MD Anderson Cancer Center

Houston, Texas, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Mei Rui, DMA

Role: CONTACT

(713) 597-1690

Facility Contacts

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Mei Rui, DMA

Role: primary

713-597-1690

Related Links

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http://www.mdanderson.org

MD Anderson Cancer Center

Other Identifiers

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NCI-2025-01927

Identifier Type: OTHER

Identifier Source: secondary_id

2024-1393

Identifier Type: -

Identifier Source: org_study_id

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