- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05949216
The Impact of Musical Engagement on Medical Resident Well-being
July 15, 2023 updated by: Conor Donnelly
It is common knowledge that music has a positive impact on human well-being.
It is also well-known that medical residents are frequently stressed and burnt out.
With these two thoughts in mind, the investigators want to explore how participating in a musical engagement program may positively impact medical resident well-being.
The investigators hope to do this by hosting four informal musical engagement sessions with medical residents, which will involve playing instruments, improvising, and reading sheet music.
To study the impact that this program has on participants, investigators will ask participants to complete a survey.
The investigators hope to find that participants are positively impacted by participation in the study, in terms of factors like stress reduction and minimized burnout symptoms.
Hopefully, the study results may inform residency program curriculum designers in the future may incorporate music into wellness programming.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
15
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Conor Donnelly, MD
- Phone Number: 6479616605
- Email: conor.donnelly@medportal.ca
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Participants will be residents in the Family Medicine program at McMaster University, in any year of study
- Participants may be on any rotation in their program schedule and located at any site
- Participants may be of any gender identity, age, ethnicity, and sexual orientation
- Must identify as a "musician", whether casual, professional, or somewhere in between - however, they require enough musical training so that they may comfortably participate in the planned sight reading and improvisation within the study
- Participants must be able to supply their own physical instrument for sessions
- Must be aged 18 or over
- Must be English-speaking
Exclusion Criteria:
- Potential participant may not be a resident of any other residency program, or be from a university other than McMaster
- If a participant is unable to participate in two or more musical sessions, they will not be included in this study
- If a participant is unable to complete the qualitative and quantitative survey forms in their entirety, they will not be included in this study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Musical engagement sessions
The single group of this study will participate in four musical engagement sessions as described in the intervention section.
|
Musical engagement sessions will be 2 hours long and involve improvisation and sight-reading of sheet music.
Participants will supply their own instrument of choice to play.
There will be four sessions total.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Improvement of burnout symptoms
Time Frame: Eight weeks
|
Participants will respond to three questionnaires - before, during, and after the study has completed.
Questions will pertain to burnout symptoms and each will use a 5-point Likert scale.
Options will be "strongly disagree", "disagree", "neutral", "agree", and "strongly disagree".
Examples of questions include "I feel burnt out" and "I have difficulty concentrating at work".
Questions will be identical between each questionnaire.
By comparing answers between surveys we will be able to determine how burnout symptoms may have changed during the course of the study.
|
Eight weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
August 1, 2023
Primary Completion (Estimated)
September 30, 2023
Study Completion (Estimated)
October 31, 2023
Study Registration Dates
First Submitted
June 28, 2023
First Submitted That Met QC Criteria
July 15, 2023
First Posted (Actual)
July 17, 2023
Study Record Updates
Last Update Posted (Actual)
July 17, 2023
Last Update Submitted That Met QC Criteria
July 15, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MRM_Study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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