- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06187272
Effectiveness of Music Practical Examinations
December 16, 2023 updated by: Christine Mulligan, Russell Sage College
Effectiveness of Music on the Performance of Graduate Occupational Therapy Students During
College student anxiety is rising alarmingly and directly affects academics, occupations, and well-being.
Occupational therapy (OT) students encounter a rigorous workload and pressure to become entry-level practitioners.
Higher education faculty strive for evidence-based teaching strategies and effective classroom management and are often challenged to promote a positive classroom culture.
This quasi-experimental study explored the effect of listening to music during a lab practical examination on the performance of OT graduate students.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Through convenience sampling, 68 graduate students in an occupational therapy program were recruited to participate.
The quasi-experimental study was conducted at Russell Sage College, in Troy, New York, with approval from the International Review Board Inclusion criteria were male and female first and second-year students, ages 19-34, enrolled in Functional Anatomy and Kinesiology or Physical Agent Modalities.
The data was collected during lab practicals in December 2021 and June 2023.
Forty-three students signed consent forms to participate.
Students sign up for 20-minute time slots in pairs for the practical exam.
Each student randomly selects confidential assessment cards and takes turns independently completing their assignment.
Each practical contains a grading rubric, and a score of 80 is required to pass.
Students either had one private room when an examiner during the practical, and either it was quiet or low 60 bpm music played in the background.
Pre and post-outcome measures evaluated each student's state, trait, test anxiety, blood pressure, and heart rate outside the assessment room.
State and trait anxiety was measured using the State-Trait Anxiety Inventory for Adults™ by Charles D. Spielberger and the Test Anxiety Inventory by Charles D. Spielberger & Associates.
State-Trait Anxiety is cited in over 20,000 articles and is the primary assessment used most often for individuals susceptible to anxiety.
The reliability of the State-Trait Anxiety is .86 - .95, and substantial evidence confirms its validity.
Mean S-anxiety .59,
T- T-anxiety .57
college students of both sexes.
The Test Anxiety Inventory measures individual situational anxiety of symptom frequency throughout an exam, like apprehension and nervousness.
Remote online survey licenses were purchased to administer the State-Trait Anxiety Adult and Test Anxiety Inventory on each student's laptop.
Mind Garden's Transform System collected raw scaled scores.
The research team recorded blood pressure and heart rate with the digital Blood Pressure monitor with an upper arm cuff.
Study Type
Interventional
Enrollment (Actual)
74
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 Locations
-
-
New York
-
Troy, New York, United States, 12180
- Russell Sage College
-
-
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
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Graduate occupational therapy students enrolled in Functional Anatomy and Kinesiology or Physical Agent Modalities
Exclusion Criteria:
- Students not registered for Functional Anatomy and Kinesiology or Physical Agent Modalities
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: Other
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Group one with no music
Graduate students with no music
|
|
Experimental: Group Two with music
Graduate students listening to music
|
Students listened to background music during a practical examination of 60 bpm.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
State-Trait Inventory
Time Frame: Day 1
|
The State-Trait Anxiety Inventory a self-report questionnaire, follows a Likert scale and measures state and trait anxiety with 40 questions and a maximum score of 80
|
Day 1
|
Test Anxiety Inventory
Time Frame: Day 1
|
The Test Anxiety Inventory is one of the most frequently used self-reported measures of situational anxiety and symptom frequency throughout an exam, like apprehension and nervousness
|
Day 1
|
Blood pressure
Time Frame: Day 1
|
The measurement of a systolic and diastolic ratio
|
Day 1
|
Heart rate
Time Frame: Day 1
|
Measuring beats per minute
|
Day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Chris Mulligan, Russell Sage College
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 (Actual)
December 7, 2021
Primary Completion (Actual)
November 28, 2023
Study Completion (Actual)
November 28, 2023
Study Registration Dates
First Submitted
November 16, 2023
First Submitted That Met QC Criteria
December 16, 2023
First Posted (Estimated)
January 1, 2024
Study Record Updates
Last Update Posted (Estimated)
January 1, 2024
Last Update Submitted That Met QC Criteria
December 16, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- RussellSage
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Consent form, study protocol, data analysis
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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